Enzymatic production of peracids using perhydrolytic enzymes

ABSTRACT

A process is provided to produce a concentrated aqueous peracid solution in situ using at least one enzyme having perhydrolase activity in the presence of hydrogen peroxide (at a concentration of at least 500 mM) under neutral to acidic reaction conditions from suitable carboxylic acid esters (including glycerides) and/or amides substrates. The concentrated peracid solution produced is sufficient for use in a variety of disinfection and/or bleaching applications.

This application is a continuation-in-part of U.S. patent application Ser. No. 11/413,246 filed Apr. 28, 2006, which claims the benefit of U.S. Provisional Application No. 60/676,116 filed Apr. 29, 2005.

FIELD OF THE INVENTION

This invention relates to the field of organic peracid synthesis and enzyme catalysis.

BACKGROUND OF THE INVENTION

Peracids have been used for disinfection in a number of applications. U.S. Pat. No. 6,545,047 B1 describes a method for sanitizing animal carcasses using antimicrobial compositions containing one or more peracids. U.S. Pat. No. 6,183,807 B1 describes a method for cleaning and sanitizing meat products using antimicrobial compositions containing one or more peracids. U.S. Pat. No. 6,518,307 B2 describes a method for controlling microbial populations in the gastrointestinal tract of animals by orally administering an effective amount of peracid. U.S. Patent Application Publication No. 20030026846 A1 describes a method of using peracid/acid compositions to control pathogenic organisms on living plant tissue. U.S. Pat. No. 5,683,724 describes a process for preventing microbial growth in aqueous streams used for transporting or processing food products and packaged foods that uses an effective antimicrobial concentration of peracid.

Peracids can be prepared by the chemical reaction of a carboxylic acid and hydrogen peroxide (see Organic Peroxides, Daniel Swern, ed., Vol. 1, pp 313-516; Wiley Interscience, New York). The reaction is usually catalyzed by a strong inorganic acid, such as concentrated sulfuric acid. The reaction of hydrogen peroxide with a carboxylic acid is an equilibrium reaction, and the production of peracid is favored by the use of an excess concentration of peroxide and/or carboxylic acid, or by the removal of water. There are several disadvantages to the chemical reaction for peracid production: a) the high concentration of carboxylic acid used to favor production of peracid can result in an undesirable odor when using the peracid-containing solution, 2) the peracid is oftentimes unstable in solution over time, and the concentration of peracid in the solution decreases during storage prior to use, and 3) the formulation is often strongly acidic due to the use of a concentrated sulfuric acid as catalyst. One way to overcome the disadvantages of the chemical production of peracids is to employ an enzyme catalyst in place of a strong acid catalyst. The use of an enzyme catalyst allows for the rapid production of peracid at the time of use, avoiding the problem of storage of peracid solutions and of using chemically-produced peracid solutions containing an unknown concentration of peracid. The high concentrations of carboxylic acids typically used to produce peracid via the direct chemical reaction with hydrogen peroxide are not required for enzymatic production of peracid, where the enzyme-catalyzed reaction can use a carboxylic acid ester or amide as substrate at a much lower concentration than is typically used in the chemical reaction. The enzyme reaction can be performed across a broad range of pH, dependent on enzyme activity and stability at a given pH, and on the substrate specificity of the enzyme for perhydrolysis at a given pH.

Enzymes can catalyze the perhydrolysis of esters and amides to produce the corresponding peroxycarboxylic acids (Equations 1 and 2), however, most known methods for preparing peracids from the corresponding carboxylic acid esters or amides using enzyme catalysts do not produce and accumulate a peracid at a sufficiently-high concentration to be efficacious for disinfection in a variety of applications.

The use of hydrogen peroxide as an enzyme substrate for the enzymatic perhydrolysis of carboxylic acid esters or amides can be problematic, as hydrogen peroxide is known to oxidatively inactivate numerous enzymes (M. R. Gray, Biotech Adv., 7:527 (1989)). K. Kleppe (Biochemistry, 5:139 (1966)) report that hydrogen peroxide inactivates enzymes by modifying certain amino acid residues in proteins, where at acid pH values methionine is easily oxidized to methionine sulfoxide, and at basic pH values tryptophan is destroyed. D. A. Estell et al. (J. Biol. Chem., 260:6518 (1985)) describe inactivation of enzymes containing methionine, cysteine or tryptophan residues by hydrogen peroxide, and demonstrate>80% inactivation of the protease subtilisin from Bacillus amyloliquefaciens in less than 6 minutes or 4 minutes using 0.1 M or 1.0 M hydrogen peroxide, respectively. Inactivation of peroxidases by 5 mM to 50 mM hydrogen peroxide is reported by M. B. Arnao et al. (Biochim. Biophys. Acta, 1041:43 (1990)), and B. Valderrama et al. (Chemistry & Biology, 9:555 (2002)) review the inactivation of peroxidases by oxidative species such as hydrogen peroxide. P. F. Greenfield et al. (Anal. Biochem., 65:109 (1975)) report an increase in inactivation of glucose oxidase with increasing hydrogen peroxide concentration. For the conversion of cephalosporin C to 7-aminocephalosporanic acid, both a D-amino acid oxidase and a glutaryl acylase were inactivated by the byproduct hydrogen peroxide produced by the oxidase (F. Lopez-Gallego, et al., Adv. Synth. Catal., 347:1804 (2005)). In view of these and other teachings, previously reported methods for enzymatic production of peracid utilize low concentrations of added hydrogen peroxide, where a low concentration of hydrogen peroxide would be expected to reduce or limit enzyme inactivation during the perhydrolysis reaction.

U.S. Pat. No. 3,974,082 (“the '082 patent”) describes the production of bleaching compositions for laundry detergent applications by contacting the material to be bleached with an aqueous solution containing an oxygen-releasing inorganic peroxygen compound, an acyl alkyl ester, and an esterase or lipase capable of hydrolyzing the ester. The bleaching compositions cited in the '082 patent are highly alkaline (using such buffering agents as pentasodium tripolyphosphate or sodium carbonate), and no data is presented for either the concentration of peracids produced in the cited compositions, or for the utility of the cited compositions for bleaching of laundry. The bleaching compositions cited in the '082 patent contain up to 40% by weight of per-compound, for example, hydrogen peroxide or alkali metal salts of percarbonate, perborate, persilicate and perphosphate. The bleaching compositions are added to water in amounts up to 12.5 grams per liter of water to initiate the enzyme-catalyzed perhydrolysis reaction, where the maximum concentration of hydrogen peroxide present in the enzyme-catalyzed perhydrolysis reaction is 5 grams/liter, equivalent to ca. 147 mM hydrogen peroxide.

U.S. Pat. No. 5,296,161 (“the '161 patent”) describes an activated oxidant system providing enhanced stain removing ability in both high and low temperature wash applications. The oxidant system is capable of in situ generation of >0.1 ppm peracid by enzymatic perhydrolysis, where in the absence of added enzyme the ester substrate is incapable of substantial chemical perhydrolysis. The oxidant system uses a source of peroxygen, a lipase or esterase, and glycerides or monoacylated ethylene glycol or propylene glycol derivatives to generate peracid. The most-preferred enzyme substrate in the '161 patent oxidant system is either trioctanoin or tridecanoin, the enzymatic reaction is carried out at a pH of from 7.5 to 11.0, and none of the accompanying examples demonstrate the production of greater than 10 ppm of peracid. The highest concentration of hydrogen peroxide present in the exemplified perhydrolysis reactions was 1314 ppm, equivalent to ca. 38.6 mM H₂O₂.

U.S. Pat. No. 5,364,554 describes an activated oxidant system for in situ generation of peracid in aqueous solution using a protease enzyme, a source of hydrogen peroxide, and an ester substrate that is preferably chemically non-perhydrolyzable. A method of bleaching and a method of forming peracid are also disclosed. The enzymatic reactions are carried out at a pH of from about 8.0 to 10.5, and none of the accompanying examples demonstrate the production of greater than 5 ppm of peracid. The concentration of hydrogen peroxide present in the exemplified perhydrolysis reactions was 400 ppm, equivalent to ca. 11.8 mM H₂O₂.

O. Kirk et al. (Biocatalysis, 11:65-77 (1994)) investigated the ability of hydrolases (lipases, esterases, and proteases) to catalyze perhydrolysis of acyl substrates with hydrogen peroxide to form peroxycarboxylic acids, and reported that perhydrolysis proceeds with a very low efficiency in aqueous systems. Furthermore, they found that lipases and esterases degraded percarboxylic acid to the corresponding carboxylic acid and hydrogen peroxide. They also found that proteases neither degraded nor catalyzed perhydrolysis of carboxylic acid esters in water. The authors concluded that esterases, lipases and proteases are, in general, not suitable for catalyzing perhydrolysis of simple esters, such as methyl octanoate and trioctanoin, in an aqueous environment.

The problem to be solved is to provide an aqueous enzymatic process for in situ production of peracid compositions under neutral to acidic conditions from non-toxic and inexpensive carboxylic acid esters, amides, and/or glycerides at concentrations suitable for use as a disinfectant or bleach in a variety of applications. Preferably, the process will produce a concentrated aqueous solution of peracid within at least about 5 minutes. As such, the enzymatic perhydrolysis process should occur in the presence of at least 500 mM hydrogen peroxide (peroxygen source). It has been reported that for certain disinfecting, cleaning or bleaching applications a non-alkaline peracid solution is preferred. As such, the process should produce an aqueous peracid solution in a single step under neutral to acidic conditions, more preferably under acidic conditions. The process preferably needs to produce peracid compositions comprised of at least 10 ppm peracid (for example peracetic acid), more preferably at least 100 ppm, and even more preferably in the range of about 100 to about 5000 ppm, where the resulting peracid composition can be used directly, or diluted to the desired concentration of peracid prior to use, to produce a 5-log or 6-log reduction in the concentration of the targeted infectious microorganism in about 5 minutes to about 10 minutes, at temperatures ranging from about 0° C. to about 60° C., preferably about 4° C. to about 30° C., most preferably about 10° C. to about 25° C.

A second problem to solve is to provide a process to produce a multi-functional composition that has disinfecting, bleaching and prion-degrading activity. The process should produce an aqueous peracid solution in situ comprising a sufficient disinfecting and/or bleaching concentrations of peracid and one or more prion-degrading proteases.

An additional problem to be solved is the lack of a combination of enzyme catalyst and enzyme substrate that results in the conversion of carboxylic acid esters or amides to percarboxylic acid at a concentration more efficacious for bleaching in laundry applications, compared to the concentrations of peracids previously disclosed in the prior art. A solution to the problem needs to 1) efficiently produce an aqueous solution of peracid where the peracid is present in sufficient concentration to act as a disinfectant or bleaching agent, 2) use an enzyme catalyst having suitable perhydrolase activity for converting carboxylic acid esters, amides, and/or glycerides to the corresponding peracids in aqueous solution; 3) provide methods to improve catalyst stability to increase the catalyst productivity, thereby decreasing catalyst cost; and 4) provide methods to efficiently and economically obtain peracids from relatively inexpensive and non-toxic starting materials.

SUMMARY OF THE INVENTION

The stated problems have been solved by providing a process to produce an aqueous peracid solution in situ using at least one enzyme having perhydrolase activity in the presence of hydrogen peroxide (at a concentration of at least 500 mM) under neutral to acidic reaction conditions from suitable carboxylic acid esters (including glycerides) and/or amides substrates. The concentration of peracid produced is sufficient for use in a variety of disinfection and/or bleaching applications.

One aspect of the invention provides a process for producing a concentrated aqueous peracid solution comprising;

-   -   a) providing a set of peracid reaction components, said         components comprising:         -   1) at least one substrate selected from the group consisting             of:             -   i) esters having the structure             -   wherein R₁=C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₂=C1 to C10 straight chain or                 branched chain alkyl group, (CH₂CH₂—O)_(n)H or                 (CH₂CH(CH₃)—O)_(n)H and n=1 to 10;             -   ii) glycerides having the structure             -   wherein R₁=C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₃ and R₄ are individually H or                 R₁C(O); and             -   iii) amides having the structure:         -   wherein R₅ and R₆═H or a C1 to C5 straight chain or branched             alkyl group;         -   2) a source of peroxygen that provides a concentration of at             least 500 mM hydrogen peroxide upon combining said reaction             components; and         -   3) at least one enzyme catalyst having perhydrolase             activity, wherein said enzyme catalyst is selected from the             group consisting of lipases, esterases, proteases, and             mixtures thereof; and     -   b) combining said reaction components at a pH of about 2.5 to         about 7.5, whereby a concentrated peracid solution is produced         within at least about 5 minutes to about 2 hours after combining         said reaction components.

This process produces a concentrated peracid solution with a peracid concentration of at least 10 ppm.

In one aspect of the invention the at least one substrate is an ester substrate selected from the group consisting of methyl lactate, ethyl lactate, methyl glycolate, ethyl glycolate, methyl methoxyacetate, ethyl methoxyacetate, methyl 3-hydroxybutyrate, ethyl 3-hydroxybutyrate, and mixtures thereof.

In another aspect of the invention the at least one substrate is a glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, and mixtures thereof.

In yet another aspect of the invention the at least one substrate is a glyceride substrate is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.

In one aspect of the invention the at least one enzyme catalyst is at least one lipase produced by an organism selected from the genera Aspergillus, Rhizopus, Penicillium, Candida, Pseudomonas, Mucor, Thermomyces, Alcaligenes, and Sus.

In another aspect the enzyme catalyst is at least one lipase selected from the group consisting of Candida antartica lipase B and Aspergillus niger lipase.

In another aspect of the invention the at least one enzyme catalyst is at least one protease with perhydrolytic activity and prion-degrading activity.

In another aspect of the invention the enzyme catalyst includes at least one lipase and at least one prion-degrading protease.

In many aspects of the invention the peracid produced by combination of the reaction components is peracetic acid.

Another aspect of the invention provides a method for disinfecting a locus having a concentration of microorganisms or viruses or combinations thereof, said method comprising:

-   -   a) providing a set of peracid reaction components, said         components comprising:         -   1. at least one substrate selected from the group consisting             of:             -   i) esters having the structure             -   wherein R₁═C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₂═C1 to C10 straight chain or                 branched chain alkyl group, (CH₂CH₂—O)_(n)H or                 (CH₂CH(CH₃)—O)_(n)H and n=1 to 10;             -   ii) glycerides having the structure             -   wherein R₁═C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₃ and R₄ are individually H or                 R₁C(O); and             -   iii) amides having the structure:         -   wherein R₅ and R₆═H or a C1 to C5 straight chain or branched             alkyl group;         -   2) a source of peroxygen that provides a concentration of at             least 500 mM hydrogen peroxide upon combining said reaction             components; and         -   3) at least one enzyme catalyst having perhydrolase             activity, wherein said enzyme catalyst is selected from the             group consisting of lipases, esterases, proteases, and             mixtures thereof;     -   b) combining said reaction components at a pH of 2.5 to 7.5,         whereby a concentrated aqueous peracid solution is formed having         a peracid concentration of at least 10 ppm within at least about         5 minutes to about 2 hours of combining said reaction         components;     -   c) optionally diluting the said aqueous peracid solution; and     -   d) contacting said locus with the aqueous peracid solution         produced in step b) or step c) whereby the concentration of said         microorganisms is reduced at least 3-log.

In another aspect of the invention the locus is contacted with the aqueous peracid solution produced in step b) or step c) as described above, within about 48 hours of combining said reaction components, or within about 5 minutes to about 48 hours.

Another aspect of the invention provides a method for decontaminating or disinfecting a locus contaminated with one or more pathogens including an infective prion or prion particle comprising

-   -   a) providing a set of peracid reaction components, said         components comprising:         -   1) at least one substrate selected from the group consisting             of:             -   i) esters having the structure             -   wherein R₁═C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₂═C1 to C10 straight chain or                 branched chain alkyl group, (CH₂CH₂—O)_(n)H or                 (CH₂CH(CH₃)—O)_(n)H and n=1 to 10;             -   ii) glycerides having the structure             -   wherein R₁═C1 to C10 straight chain or branched chain                 alkyl optionally substituted with an hydroxyl or a C1 to                 C4 alkoxy group and R₃ and R₄ are individually H or                 R₁C(O); and             -   iii) amides having the structure:         -   wherein R₅ and R₆═H or a C1 to C5 straight chain or branched             alkyl group;         -   2) a source of peroxygen that provides a concentration of at             least 500 mM hydrogen peroxide upon combining said reaction             components; and         -   3) at least one enzyme catalyst having perhydrolase             activity, wherein said enzyme catalyst is selected from the             group consisting of lipases, proteases, and mixtures             thereof;         -   4) at least one prion-degrading protease wherein one or more             of the prion-degrading proteases may be the same as the             enzyme catalyst providing the perhydrolase activity in             (a)(3);     -   b) combining said reaction components at a pH of 2.5 to 7.5,         whereby a concentrated peracid solution is produced having a         peracid concentration of at least 10 ppm within at least about 5         minutes to about 2 hours of combining said reaction components;         and     -   c) optionally diluting said peracid solution produced in step         (b).     -   d) contacting a locus contaminated with a microorganism, a         virus, a prion or prion particle, or a combination thereof with         the aqueous peracid solution produced in step b) or step c)         whereby said locus is disinfected and said prion particle is         degraded.

Another aspect of the invention provides a concentrated peracid solution produced in situ by the process described above, wherein said solution includes at least one protease suitable for prion degradation.

Yet another aspect of the invention provides a multifunctional disinfectant composition comprising the concentrated peracid solution produced by the process described above, wherein said composition is suitable for prion degradation, use as a biocide, use as a virucide, or combinations thereof.

In yet another embodiment, a biocidal composition having prion-degrading activity and components suitable for producing an effective amount of peracid in situ is also provided, said composition comprising components suitable for producing peracid in situ, wherein said components comprise one or more prion-degrading enzymes, a suitable substrate, at least one enzyme having perhydrolase activity, and a source of peroxygen.

DETAILED DESCRIPTION OF THE INVENTION

The stated problems have been solved by the discovery of a combination of enzymes and carboxylic acid esters or amides that, in the presence of an inorganic source of peroxygen (for example, hydrogen peroxide), produce concentrations of peracids sufficient for disinfection or bleaching applications. It was unexpected that concentrations of hydrogen peroxide of from about 500 mM to about 2500 mM could be employed in enzyme-catalyzed perhydrolysis reactions to generate peracid in concentrations of as high as 5000 ppm in 5-10 minutes, where these high peroxide concentrations were expected to rapidly inactivate the perhydrolytic enzyme catalyst.

When compared to the concentrations of peracids produced by the enzymatic perhydrolysis of esters previously reported, the combination of the present enzymes and enzyme substrates in the concentration ranges reported herein unexpectedly and efficiently produced an aqueous solution of peracid at a sufficiently-high concentration to act as a biocidal and virucidal disinfectant, as well as a bleaching agent. Concentrations of peracids in excess of 10 ppm (generally greater than about 75 ppm) were produced as described herein using enzyme catalysts (e.g., lipases, proteases), where the resulting peracid-containing solution, or a dilution thereof, can effect a 5-log or 6-log reduction in infectious bacteria in 5 minutes to 10 minutes at about 25° C.

PCT Publication No. WO2004039418 Al and U.S. Pat. 6,613,505 B2 describe a method and composition for destruction of infectious prion proteins in tissue by thermal/enzymatic treatment of the tissue with a prion-destructive protease. U.S. Patent Appl. Pub. No. 2006/0127390 A1 describes a method for inactivating agents that cause transmissible spongiform encephalopathies (also called prion diseases), where the transmissible spongiform encephalopathy agent is contacted with a subtilisin protease. U.S. Patent Appl. Pub. No. 2006/0030505 A1 describes a method for inactivating prions using a composition having a peracid alone, or a peracid and a surfactant; these compositions may optionally include one or more enzymes, where the enzymes provide desirable activity for removal of protein-based, carbohydrate-based, or triglyceride-based soil from substrates. Co-filed provisional patent application (Attorney docket number CL3735, titled LOW TEMPERATURE PRION DECONTAMINATION), filed on Oct. 27, 2006, describes the use of a mixture of Alcalase and Neutrase in combination with peracid to inactivate prions, herein specifically incorporated by reference.

In another aspect of the invention, cleaning and disinfecting compositions are provided comprising prion-degrading proteases in combination with in situ generated peracid concentrations having biocidal and/or virucidal activity. In yet another aspect, the prion-degrading proteases (e.g., Proteinase K, Pronase, Alcalase® (a subtilisin protease), and Neutrase® (a metallo-endopeptidase, also known as a neutral protease), are capable of catalyzing the perhydrolysis of esters and/or amides to produce the corresponding peracid at concentrations efficacious for disinfection, thereby creating a biocide and/or virucide having prion-degrading activity. Savinase®, Polarzyme®, Everlase® and combinations thereof) are also capable of catalyzing the perhydrolysis of esters and/or amides to produce the corresponding peracid at concentrations efficacious for disinfection, thereby creating a biocide and/or virucide that may also have prion-degrading activity. In a further aspect of the invention, prion-degrading proteases may be used in combination with an added enzyme having perhydrolytic activity, such as a lipase, at a pH where the protease(s) alone may not produce an efficacious concentration of peracid (e.g., at pH of from 4.0 to 6.5). This combination may also yield a synergistic concentration of peracid, where the peracid is produced in a concentration that is greater than the sum of peracid produced by either protease or lipase alone.

Unless otherwise stated, all references cited are hereby specifically incorporated by reference. Further, when an amount, concentration, or other value or parameter is given either as a range, preferred range, or a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range. It is not intended that the scope of the invention be limited to the specific values recited when defining a range.

In this disclosure, a number of terms and abbreviations are used. The following definitions apply unless specifically stated otherwise.

As used herein, the term “about” modifying the quantity of an ingredient or reactant of the invention employed refers to variation in the numerical quantity that can occur, for example, through typical measuring and liquid handling procedures used for making concentrates or use solutions in the real world; through inadvertent error in these procedures; through differences in the manufacture, source, or purity of the ingredients employed to make the compositions or carry out the methods; and the like. The term “about” also encompasses amounts that differ due to different equilibrium conditions for a composition resulting from a particular initial mixture. Whether or not modified by the term “about”, the claims include equivalents to the quantities. In one embodiment, the term “about” means within 10% of the reported numerical value, preferably with 5% of the reported numerical value.

As used herein, the term “comprising” means the presence of the stated features, integers, steps, or components as referred to in the claims, but that it does not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.

As used herein, the term “peracid” is synonymous with peroxyacid, peroxy acid, percarboxylic acid and peroxoic acid. As is commonly known, peracid includes peracetic acid.

As used herein, the term “peracetic acid” is abbreviated as “PM” and is synonymous with peroxyacetic acid, ethaneperoxoic acid and all other synonyms of CAS Registry Number 79-21-0.

The term “triacetin” is synonymous with glycerin triacetate; glycerol triacetate; glyceryl triacetate, 1,2,3-triacetoxypropane, 1,2,3-propanetriol triacetate and all other synonyms of CAS Registry Number 102-76-1.

As used herein, the terms “suitable enzymatic reaction mixture”, “components suitable for in situ generation of a peracid”, and “suitable reaction components” refer to the materials and water in which the reactants and enzyme catalyst come into contact. The components of the suitable aqueous reaction mixture are provided herein and those skilled in the art appreciate the range of component variations suitable for this process. In one embodiment, the suitable enzymatic reaction mixture produces peracid in situ upon combining the reaction components. As such, the reaction components may be provided as a multicomponent system wherein one or more of the reaction components remains separated until use. The design of systems for combining multiple active components are known in the art and generally will depend upon the physical form of the individual reaction components. For example, multiple active fluids (liquid-liquid) systems typically use multichamber dispenser bottles or two-phase systems (U.S. Patent Appln. Pub. No. 2005/0139608; U.S. Pat. No. 5,398,846; U.S. Pat. No. 5,624,634; U.S. Pat. No. 6,391,840; E.P. Patent No. 0807156B1; U.S. Patent Appln. Pub. No. 2005/0008526; and PCT Publication No. WO 00/11713A1) such as found in some bleaching applications wherein the desired bleaching agent is produced upon mixing the reactive fluids. Other forms of multicomponent systems used to generate peracid may include, but are not limited to those designed for one or more solid components or combinations of solid-liquid components, such as powders (e.g., many commercially available bleaching composition, U.S. Pat. No. 5,116,575), multi-layered tablets (U.S. Pat. No. 6,210,639), water dissolvable packets having multiple compartments (U.S. Pat. No. 6,995,125) and solid agglomerates that react upon the addition of water (U.S. Pat. No. 6,319,888).

As used herein, the term “perhydrolysis” is defined as the reaction of a selected substrate with peroxide to form a peracid. Typically, an inorganic peroxide is reacted with the selected substrate in the presence of a catalyst to produce the peracid. As used herein, the term “chemical perhydrolysis” includes perhydrolysis reactions in which a substrate (a peracid precursor) is combined with a source of hydrogen peroxide wherein peracid is formed in the absence of an enzyme catalyst. As used herein, the term “enzymatic perhydrolysis” refers to a perhydrolysis reaction that is assisted or catalyzed by an enzyme generally classified as a hydrolase.

“Carboxylic ester hydrolase” refers to an enzyme that catalyzes the hydrolysis of an ester (E.C. 3.1.1.-). The carboxylic ester hydrolase family includes, but is not limited to lipases (e.g., triacylglycerol lipases [E.C. 3.1.1.3]) and esterases.

“Lipase” refers to an enzyme that catalyzes the hydrolysis of fats into glycerol and fatty acids by hydrolyzing ester bonds (EC 3.1.1.3). Some lipases have been reported to have perhydrolysis activity.

“Esterase” refers to an enzyme that catalyzes the hydrolysis of an ester (EC 3.1.1.-). Some esterases have been reported to have perhydrolysis activity

“Protease” refers to an enzyme that catalyzes the hydrolytic breakdown of proteins via hydrolysis of peptide bonds (EC 3.4.-). As described herein, some proteases exhibit perhydrolysis activity.

As used herein, the terms “perhydrolase catalyst”and “at least one suitable enzyme catalyst having perhydrolase activity” refer herein to an enzyme catalyst that is characterized by perhydrolase activity. The enzyme catalyst is selected from the group consisting of lipases, esterases, proteases, and/or mixtures thereof wherein the catalyst has perhydrolysis activity. The enzyme catalyst may be in the form of a whole microbial cell, permeabilized microbial cell(s), one or more cell components of a microbial cell extract, partially purified enzyme, or purified enzyme. As used herein, the term “produced from an organism” is used to describe the source of the suitable catalyst. The enzyme catalyst may be produced from the target organism or may be recombinantly produced in a suitable production host.

As used herein, “one unit of enzyme activity” or “one unit of activity” or “U” is defined as the amount of enzyme activity required for the production of 1 μmol of peracid product per minute at a specified temperature.

As used herein, the term “perhydrolase activity” refers to the enzyme activity per unit mass (for example, milligram) of protein, solid or liquid enzyme-containing composition, dry cell weight, or immobilized catalyst weight. Comparisons of perhydrolase activity of catalysts were determined proportional to the dry cell weight, solid or liquid enzyme-containing composition or protein catalyst weight.

As used herein, the term “disinfect” refers to the process of cleansing so as to destroy or prevent the growth of pathogenic microorganisms. As used herein, the term “disinfectant” refers to an agent that disinfects by destroying, neutralizing, or inhibiting the growth of disease-carrying microorganisms. Typically disinfectants are used to treat inanimate objects or surfaces. As used herein, the term “antiseptic” refers to a chemical agent that inhibits the growth of disease-carrying microorganisms.

As used herein, the term “virucide” refers to an agent that inhibits or destroys viruses. An agent that exhibits the ability to inhibit or destroy viruses is described as having “virucidal” activity. Peracids can have virucidal activity. Typical alternative virucides known in the art which may be suitable for use with the present invention include, for example, alcohols, ethers, chloroform, formaldehyde, phenols, beta propiolactone, iodine, chlorine, mercury salts, hydroxylamine, ethylene oxide, ethylene glycol, quaternary ammonium compounds, enzymes, and detergents

As used herein, the term “biocide” refers to a chemical agent, typically broad spectrum, which inactivates or destroys microorganisms. A chemical agent that exhibits the ability to inactivate or destroy microorganisms is described as having “biocidal” activity. Peracids can have biocidal activity. Typical alternative biocides known in the art, which may be suitable for use in the present invention include, for example, chlorine, chlorine dioxide, chloroisocyanurates, hypochlorites, ozone, acrolein, amines, chlorinated phenolics, copper salts, organo-sulphur compounds, and quaternary ammonium salts.

As used herein, the phrase “minimum biocidal concentration” refers to the minimum concentration of a biocidal agent that, for a specific contact time, will produce a desired lethal, irreversible reduction in the viable population of the targeted microorganisms. The effectiveness can be measured by the log₁₀ reduction in viable microorganisms after treatment. In one aspect, the targeted reduction in viable cells after treatment is a 3-log reduction, more preferably a 4-log reduction, and most preferably at least a 5-log reduction. In another aspect, the minimum biocidal concentration is a 6-log reduction in viable microbial cells.

As used herein, the terms “prion”, “prion particle”, and “infection prion particle” refer to infectious proteins associated with neurodegenerative diseases including, but not limited to scrapie, bovine spongiform encephalopathy (BSE), trasmissible spongiform encephalopathy (TSE), chronic wasting disease, and Creutzfeldt-Jacob disease. The term “prion-destructive protease” or “prion-degrading protease” refers to at least one protease (preferably combinations of two or more proteases) useful for degrading or destroying infectious prion particles (for example, see WO 2004039418 A1 and US 20020172989 A1). In one embodiment, the prion-destructive protease is selected from Proteinase K, Pronase, and mixtures thereof. In a preferred embodiment, the prion-destructive protease is a mixture of Proteinase K and Pronasee. In a further preferred embodiment, the prion-destructive protease is selected from Alcalase®, Neutrase®, and mixtures thereof. In an additional preferred embodiment, Savinase®, Polarzyme®, and Everlase®, and mixtures thereof, are employed as perhydrolytic enzymes, where these proteases, individually, or in combination, may also degrade prions. In yet a further preferred embodiment, the prion-destructive protease is a mixture of Alcalase® and Neutrase®.

In one aspect, the peracids formed by the present process can be used to reduce a microbial population when applied on and/or at a locus. As used herein, a “locus” of the invention comprises part or all of a target surface suitable for disinfecting or bleaching. Target surfaces include all surfaces that can potentially be contaminated with microorganisms, viruses, prions or combinations thereof. Non-limiting examples include equipment surfaces found in the food or beverage industry (such as tanks, conveyors, floors, drains, coolers, freezers, equipment surfaces, walls, valves, belts, pipes, drains, joints, crevasses, combinations thereof, and the like); building surfaces (such as walls, floors and windows); non-food-industry related pipes and drains, including water treatment facilities, pools and spas, and fermentation tanks; hospital or veterinary surfaces (such as walls, floors, beds, equipment, (such as endoscopes) clothing worn in hospital/veterinary or other healthcare settings, including scrubs, shoes, and other hospital or veterinary surfaces); restaurant surfaces; bathroom surfaces; toilets; clothes and shoes; surfaces of barns or stables for livestock, such as poultry, cattle, dairy cows, goats, horses and pigs; and hatcheries for poultry or for shrimp. Additional surfaces also include food products, such as beef, poultry, pork, vegetables, fruits, seafood, combinations thereof, and the like. The locus can also include water absorbent materials such as infected linens or other textiles. The locus also includes harvested plants or plant products including seeds, corms, tubers, fruit, and vegetables, growing plants, and especially crop growing plants, including cereals, leaf vegetables and salad crops, root vegetables, legumes, berried fruits, citrus fruits and hard fruits.

Non-limiting examples of surface materials are metals (e.g., steel, stainless steel, chrome, titanium, iron, copper, brass, aluminum, and alloys thereof), minerals (e.g., concrete), polymers and plastics (e.g., polyolefins, such as polyethylene, polypropylene, polystyrene, poly(meth)acrylate, polyacrylonitrile, polybutadiene, poly(acrylonitrile, butadiene, styrene), poly(acrylonitrile, butadiene), acrylonitrile butadiene; polyesters such as polyethylene terephthalate; and polyamides such as nylon). Additional surfaces include brick, tile, ceramic, porcelain, wood, vinyl, linoleum, and carpet.

Suitable Aqueous Reaction Conditions for the Enzyme-Catalyzed Preparation of Peracids from Carboxylic Acid Esters and/or Amides and Hydrogen Peroxide

A process is provided to produce an aqueous mixture comprising a peracid by reacting a suitable substrate, at least one enzyme catalyst having perhydrolysis activity, and a source of peroxygen providing a hydrogen peroxide concentration of 500 mM or more at a neutral to acidic pH. As used herein, the terms “peroxygen source” and “source of peroxygen” refer to compounds capable of providing hydrogen peroxide at a concentration of about 500 mM or more when in an aqueous solution including, but not limited to hydrogen peroxide, hydrogen peroxide adducts, perborates, and percarbonates. As described herein, the peroxygen source is capable of providing, upon combining the reaction components, a mixture having a hydrogen peroxide concentration of at least 500 mM.

As used herein, the terms “suitable, substrate”, “peracid precursor”, and “bleach activator” will be used to describe substrates capable of undergoing enzymatic perhydrolysis to generate a peracid using the present reaction conditions. The substrates may also undergo partial chemical perhydrolysis in the presence or absence of enzyme. As such, substrates suitable in the present invention are those that can undergo enzymatic perhydrolysis to generate at least 10 ppm more peracid then that produced chemically under identical reaction conditions, preferably at least 100 ppm, more preferably at least 250 ppm, even more preferably at least 500 ppm, yet even more preferably at least 1000 ppm, still even more preferably at least 2000 ppm, and most preferably at least 5000 ppm peracid.

Suitable substrates may include one or more carboxylic acid esters, amides, glycerides (mono-, di-, and/or triglycerides) or mixture thereof capable of undergoing enzymatic perhydrolysis under the present reaction conditions. In one embodiment, the substrate may be optionally substituted, especially with alkoxy and/or hydroxyl groups. In another embodiment, the substrate may be a acylated polyol. In yet another embodiment, the acylated polyol is selected from the group consisting of mono-, di- or polyacylated polyols derived from glycerol, erythritol, threitol, xylitol, ribitol, arabitol, mannitol, and sorbitol.

In a preferred embodiment, suitable substrates include carboxylic acid esters, amides, and/or glycerides having a formula selected from the group consisting of:

-   -   a) esters of the formula         wherein R₁═C1 to C10 strain chain or branched chain alkyl         optionally substituted with an hydroxyl or a C1 to C4 alkoxy         group and R₂═C1 to C10 strain chain or branched chain alkyl         group, (CH₂CH₂—O)_(n)H or (CH₂CH(CH₃)—O)_(n)H and n=1 to 10;     -   b) glycerides of the formula         wherein R₁=C1 to C10 straight chain or branched chain alkyl         optionally substituted with an hydroxyl or a C1 to C4 alkoxy         group and R₃ and R₄ are individually H or R₁C(O); and     -   c) amides of the formula         wherein R₅ and R₆═H or a C1 to C5 straight chain or branched         alkyl group. In one embodiment, the substrate may be a mixture         of one or more suitable substrates as described herein.

In a preferred embodiment, the substrates are selected from the group consisting of methyl lactate, ethyl lactate, methyl glycolate, ethyl glycolate, methyl methoxyacetate, ethyl methoxyacetate, methyl 3-hydroxybutyrate, ethyl 3-hydroxybutyrate, triethyl 2-acetyl citrate, glucose pentaacetate, gluconolactone, monoacetin, diacetin, triacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, acetamide, diacetamide, and mixtures thereof.

In yet a further preferred embodiment, the substrate is selected from the group consisting of monoacetin, diacetin, triacetin, acetamide, diacetamide, and mixtures thereof.

The enzyme substrate is present in the reaction mixture at a concentration sufficient to produce the desired concentration of peracid upon enzyme-catalyzed perhydrolysis. It has been demonstrated in the accompanying examples that there are preferred combinations of enzyme substrate and enzyme catalyst that produce a desirable concentration of peracid. The substrate need not be completely soluble in the reaction mixture, but have sufficient solubility to permit conversion of the ester or amide by the enzyme catalyst to the corresponding peracid. The substrate is present in the reaction mixture at a concentration of 0.05 wt % to 40 wt % of the reaction mixture, preferably at a concentration of 0.1 wt % to 20 wt % of the reaction mixture, and more preferably at a concentration of 0.5 wt % to 10 wt % of the reaction mixture. Preferred substrates when using a lipase, esterase, or protease as catalyst, or combinations of lipases and/or proteases as catalyst, include monoacetin, diacetin, triacetin, and mixtures of monoacetin/diacetin/triacetin. Additional preferred substrates when using a protease as catalyst, or combinations of lipases and proteases as catalyst, include acetamide, diacetamide, and mixtures thereof.

The peroxygen source may include, but is not limited to, hydrogen peroxide, perborate salts (e.g., sodium perborate) and percarbonate salts (e.g. sodium percarbonate). The concentration of peroxygen compound in the reaction mixture may range from 0.1 wt % to about 50 wt %, preferably from 1 wt % to about 40 wt %, more preferably from 2 wt % to about 30 wt %

The concentration of the hydrogen peroxide provided by the peroxygen compound in the aqueous reaction mixture is initially at least 500 mM or more upon combining the reaction components. In one embodiment, the hydrogen peroxide concentration in the aqueous reaction mixture is 1000 mM or more. In another embodiment, the hydrogen peroxide concentration in the aqueous reaction mixture is 2500 mM or more.

The molar ratio of the hydrogen peroxide to substrate (H₂O₂:substrate) in the aqueous reaction mixture may be from about 0.1 to 20, preferably about 0.5 to 10, and most preferably about 2 to 5.

The reaction components may be combined in individual batches or may be combined using a continuous process.

The enzyme catalyst is chosen from the class of hydrolytic enzymes that includes esterases, lipases and proteases (EC 3.1.1.-, EC 3.1.1.3, and EC 3.4.-.-, respectively). In particular, the enzymes that are useful in the present invention are hydrolytic enzymes, such as esterases, lipases, and proteases, whose catalytic activity is normally the hydrolysis of an ester to the corresponding carboxylic acid and alcohol, or the hydrolysis of an amide to the corresponding carboxylic acid and ammonia or amine, where in the presence of hydrogen peroxide (or a functionally-equivalent peroxygen containing compound) the ester or amide is subject to an enzyme-catalyzed perhydrolysis, producing the corresponding percarboxylic acid.

In one aspect, the enzyme catalyst is a lipase derived from a eukaryotic or prokaryotic organism. In another aspect, the lipase is derived from an organism selected from the genera consisting of Aspergillus, Rhizopus, Penicillium, Candida, Pseudomonas, Mucor, Thermomyces, Alcaligenes, and Sus. In a preferred aspect, the source of the lipase is selected from the group consisting of Aspergillus niger, Rhizopus oryzae, Penicillium sp. I, Penicillium sp. II, Candida rugosa, Candida antartica lipase A, Candida antartica lipase B, Pseudomonas cepacia, Pseudomonas fluorescens, Thermomyces languinosus, Mucor miehei, Sus scrofa, and Alcaligenes sp. In a further preferred aspect, the lipase is selected from the group consisting of Aspergillus sp. lipase, Aspergillus niger lipase, Candida antartica lipase B, Pseudomonas sp. lipase, Alcaligenes sp. lipase, Candida rugosa lipase, Rhizopus oryzae lipase, and mixtures thereof. Many of the lipases of exemplified herein were obtained from BioCatalytics Inc. (Pasadena, Calif.) and referred to by their corresponding catalog number (Example 1, Table 1). Accordingly, in a further preferred aspect, the lipase is selected from the group consisting of ICR-101 Aspergillus sp. lipase, ICR-102 Rhizopus sp. lipase, ICR-103 Rhizopus oryzae lipase, ICR-104 Penicillium sp. I lipase, ICR-105 Penicillium sp. II lipase, ICR-106 Candida rugosa lipase, ICR-107 Pseudomonas cepacia lipase, ICR-108 Pseudomonas sp. lipase, ICR-109 Pseudomonas fluorescens lipase, ICR-110 Candida antartica lipase B, ICR-111 Candida sp. lipase, ICR-112 Candida antartica lipase A, ICR-113 Pseudomonas sp. lipase, ICR-114 porcine pancreas lipase, ICR-115 Thermomyces languinosus lipase, ICR-116 Mucormiehei lipase, and ICR-117 Alcaligenes sp. lipase. In a further preferred aspect, the lipase is selected from the group consisting of Lipase AY “Amano”30 (Candida rugosa lipase), Lipase R “Amano”(Penicillium roqueforti lipase), Lipase F-AP15 (Rhizopus oryzae lipase), Lipase M “Amano”10 (Mucor javanicus lipase), Lipase A “Amano”12 (Aspergillus niger lipase), Lipase G “Amano” 50 (Penicillium camembertii lipase), Amano F-DS lipase (Rhizopus oryzae lipase), Amano DS lipase (Aspergillus niger lipase) (all from Amano), and CALB L (liquid formulation of Candida antartica lipase B), Novozym 435 (immobilized Candida antartica lipase B), Lipozyme TL (Thermomyces lanuginosus lipase), Palatase 20000L (Aspergillus oryzae lipase) (all from Novozymes), and Validase AN lipase (Aspergillus niger lipase), Dietrenz CR lipase (Candida rugosa lipase) (all from Valley Research), and Enzeco MLC lipase (a microbial lipase concentrate from Aspergillus niger sold by Enzyme Development Corporation. Most preferably, the lipase is selected form the group consisting of BioCatalytics ICR-101 (Aspergillus sp. lipase), BioCatalytics ICR-110 (Candida antartica lipase B),BioCatalytics Chirazyme L2 lipase (C. antartica lipase B), BioCatalytics ICR-1 13 (Pseudomonas sp. lipase), BioCatalytics CR-1 17 (Alcaligenes sp. lipase), Lipase A “Amano”12 (Aspergillus niger lipase), Novozym CALB L (Candida antartica lipase B), Novozym 435 (immobilized Candida antartica lipase B), Novozym Palatase 20000L (Aspergillus oryzae lipase), and Valley Research Validase AN (Aspergillus nigerlipase).

In one embodiment, the enzyme catalyst is a protease (E.C. 3.4.-.-) derived from a eukaryotic or prokaryotic organism. In another embodiment the protease is derived from an organism selected from the genera consisting of Aspergillus, Streptomyces, Tritirachium, Rhizopus, Bacillus, Sus, Carica, Ananas, Pseudomonas, Mucor, Thermomyces, Alcaligenes, and Sus. In a preferred aspect, the source of the protease is selected from the group consisting of Aspergillus saitoi, Rhizopus sp, Bacillus sp., Bacillus subtilis, Sus scrofa (pig), Carica papaya (papaya), Ananas comosus (pineapple), Streptomyces griseus, and Tritirachium album. In a preferred embodiment, the protease is selected from the group consisting of the Aspergillus saitoi type XIII protease, Rhizopus sp. type XVIII protease, Bacillus sp. (e.g. Bacillus subtilis, Bacillus amyloliquefaciens, Bacillus licheniformis, Bacillus lentus, etc.) proteases such as subtilisin (Alcalase®; available from Novozymes), the neutral protease (Neutrase®; available from Novozymes), (Savinase®; available from Novozymes), Sus scrofa pepsin, Carica papaya Chymopapain, Ananas comosus bromelain, Carica papaya papain, Streptomyces griseus Pronase (also known as Pronase E® or Pronase®), Tritirachium album Proteinase K (including recombinantly produced Proteinase K from Pichia pastoris), and mixtures thereof.

Many enzyme catalysts (whole cell, partially purified, or purified) have been reported to have catalase activity (EC 1.11.1.6). Catalases catalyze the conversion of hydrogen peroxide into oxygen and water. In a preferred embodiment, the enzyme catalyst lacks significant catalase activity or is engineered or purified to decrease or eliminate catalase activity.

The concentration of enzyme catalyst employed in the aqueous reaction mixture depends in part on the specific catalytic activity of the enzyme catalyst, and is chosen to obtain the desired rate of reaction. The weight of soluble enzyme used as catalyst in perhydrolysis reactions typically ranges from 0.01 mg to 10 mg of enzyme per mL of total reaction volume, preferably from 0.10 mg to 2.0 mg of enzyme per mL. The enzyme may also be immobilized on a soluble or insoluble support using methods well-known to those skilled in the art; see for example, Immobilization of Enzymes and Cells; Gordon F. Bickerstaff, Editor; Humana Press, Totowa, N.J., USA; 1997. The use of immobilized enzymes permits the recovery and reuse of the catalyst in subsequent reactions. Additional forms of the enzyme catalyst that are useful in the present application include whole microbial cells, cell extracts, and partially-purified enzymes. These additional forms of the catalyst may also be immobilized using the methods referenced above.

In one aspect, the concentration of peracid generated by the combination of chemical perhydrolysis and enzymatic perhydrolysis of the substrate is sufficient to provide an effective concentration of peracid for bleaching or disinfection at a desired pH. In another aspect, the present methods provide combinations of enzymes and enzyme substrates to produce the desired effective concentration of peracid, where, in the absence of added enzyme, there is a significantly lower concentration of peracid produced. Although there may in some cases be substantial chemical perhydrolysis of the enzyme substrate by direct chemical reaction of inorganic peroxide with the enzyme substrate, there may not be a sufficient concentration of peracid generated to provide an effective concentration of peracid in the desired applications, and a significant increase in total peracid concentration is achieved by the addition of an appropriate enzyme catalyst to the reaction mixture.

The present process produces a concentrated aqueous peracid solution that may be optionally diluted (e.g., with water) prior to use. As used herein, “peracid solution”, “aqueous peracid solution”, and “concentrated aqueous peracid solution” will refer to the concentrated peracid solution generated by the present enzyme-catalyzed perhydrolysis process. In one embodiment, the “concentrated aqueous peracid solution” comprises at least 10 ppm peracid, preferably at least 100 ppm peracid, more preferably at least 200 ppm peracid, even more preferably at least 250 ppm peracid, yet even more preferably at least 500 ppm, still yet even more preferably at least 1000 ppm, yet even more preferably at least 2000 ppm, and most preferably at least 5000 ppm. The product mixture comprising the peracid may be optionally diluted with water, or a solution predominantly comprised of water, to produce a mixture with the desired lower concentration of peracid. The decision to dilute the aqueous peracid solution produced by the present method will depend upon a variety of factors including, but not limited to the target application (animal health disinfectant, instrument sterilization, household cleaner, bleaching agent, etc.), temperature and time required to ensure the desired level efficacy for the target application, the amount of soil at and/or on the target locus, and the target pathogen's susceptibility to peracid disinfectants. The reaction time required to produce the desired concentration of peracid is not greater than about two hours, preferably not greater than about 30 minutes, more preferably not greater than about 10 minutes, and most preferably less than or about 5 minutes. As the reaction continues, the concentration of peracid will increase to the point of equilibrium. As such, the present invention is directed to a process that produces a high concentration within about 5 minutes, said concentration may continue to rise until an equilibrium of the reaction is reached.

The temperature of the peracid synthesis reaction is chosen to control both the reaction rate and the stability of the enzyme catalyst activity. The temperature of the reaction may range from just above the freezing point of the reaction mixture (approximately 0° C.) to about 65° C., with a preferred range of reaction temperature of from about 5° C. to about 35° C.

The pH of the final reaction mixture (i.e., pH of the reaction mixture upon combining the reaction components) containing peracid is 2.5 to 7.5, preferably from 3 to 7, more preferably from 3.5 to 6.5, and most preferably 4 to 6.5. The pH of the reaction, and of the final reaction mixture, may optionally be controlled by the addition of a suitable buffer, including, but not limited to phosphate, pyrophosphate, bicarbonate, acetate, or citrate. The concentration of buffer is from 0.1 mM to 1.0 M, preferably from 1 mM to 100 mM, most preferably from 10 mM to 50 mM.

In another aspect, the enzymatic perhydrolysis product may contain additional components that provide desirable functionality. These additional components include, but are not limited to detergent builders, emulsifiers, surfactants, corrosion inhibitors, enzyme stabilizers, and peroxide stabilizers (e.g., metal ion chelating agents). Many of the additional components are well know in the detergent industry (see for example U.S. Pat. No. 5,932,532 hereby incorporated by reference). Examples of emulsifiers include polyvinyl alcohol or polyvinylpyrrolidine. Examples of surfactants, including a) non-ionic surfactants such as block copolymers of ethylene oxide or propylene oxide, ethoxylated or propoxylated linear and branched primary and secondary alcohols, and aliphatic phosphine oxides b) cationic surfactants such as such as quaternary ammonium compounds, particularly quaternary ammonium compounds having a C8-C20 alkyl group bound to a nitrogen atom additionally bound to three C1-C2 alkyl groups, c) anionic surfactants such as alkane carboxylic acids (e.g., C8-C20 fatty acids), alkyl phosphonates, alkane sulfonates (e.g., sodium dodecylsulphate “SDS”) or linear or branched alkyl benzene sulfonates, alkene sulfonates and d) amphoteric and zwitterionic surfactants such as aminocarboxylic acids, aminodicarboxylic acids, and alkybetaines. Additional components may include fragrances, dyes, stabilizers of hydrogen peroxide (e.g., 1-hydroxyethylidene-1,1-diphosphonic acid (Dequest 2010, Solutia Inc., St. Louis, Mo.)), stabilizers of enzyme activity (e.g., polyethyleneglycol (PEG)), detergent builders and metal chelators (e.g., ethylenediaminetetraacetic acid (EDTA)).

Enzymatic In Situ Production of Peracids

The present aqueous enzymatic method produces high concentrations of peracid or peracids in situ. The peracids produced are quite reactive and relatively unstable, generally decreasing in concentration over time. As such, it may be desirable to keep the various reaction components separated, especially for liquid formulations. In one aspect, the hydrogen peroxide source is separate from either the substrate or the enzyme, preferably from both. This can be accomplished using a variety of techniques including, but not limited to the use of multicompartment chambered dispensers (U.S. Pat. No. 4,585,150) and physically combining the enzyme catalyst with the present substrates and hydrogen peroxide source to initiate the aqueous enzymatic perhydrolysis reaction. The enzyme catalyst may be immobilized within the body of the reaction chamber or separated (e.g. filtered, etc.) from the reaction product comprising the peracid prior to contacting the surface and/or object targeted for treatment. The enzyme catalyst may be in a liquid matrix or in a solid form (i.e. powdered, tablet) or embedded within a solid matrix that is subsequently mixed with the substrates and hydrogen peroxide source to initiate the enzymatic perhydrolysis reaction. In a further aspect, the enzyme catalyst may be contained within a dissolvable or porous pouch that may be added to the aqueous substrate matrix to initiate enzymatic perhydrolysis.

HPLC Assay Method for Determining the Concentration of Peracid and Hydrogen Peroxide.

A variety of analytical methods can be used in the present method to analyze the reactants and products including, but not limited to titration, high performance liquid chromatography (HPLC), gas chromatography (GC), mass spectroscopy (MS), and capillary electrophoresis (CE).

The analytical procedure described by U. Karst et al. (Anal. Chem., 69 (17):3623-3627 (1997)) was employed, as described herein, for analysis of product mixtures containing peracid and hydrogen peroxide. Briefly, the concentration of peracetic acid (PAA) in analyzed samples ranged from 0.025 mM-10 mM, and the concentration of H₂O₂ ranged from 0.075 mM-3 mM. Reaction mixtures containing peracid and/or hydrogen peroxide were, if necessary prior to analysis, diluted to produce a concentration of peracid or peroxide in these ranges. Into a 4-mL vial was placed 0.100 mL of 20 mM methyl p-tolyl sulfide (MTS) in acetonitrile, 0.300 mL of distilled and deionized water (dd) and 0.100 mL of sample solution (undiluted or diluted with dd water by a factor of up to 1:25 for analysis of peracid), or 0.100 mL of 20 mM MTS in acetonitrile and 0.390 mL of dd water were added to 0.010 mL of a 1:10 dilution of sample solution (for analysis of hydrogen peroxide). After a reaction time of 10 minutes (in the dark, with no stirring), 0.400 mL CH₃CN and 0.100 mL of 40-mM triphenylphosphine (TPP) in CH₃CN were added to start the second derivatization reaction for detection of peroxide. The solution was left standing in the dark for 30 min to complete the assay reaction. At the end of 30 minutes, 0.100 mL of 10 mM N,N-diethyl-m-toluamide (DEET, HPLC external standard) was added and the resulting solution analyzed by HPLC: Supelco Discovery C8 10-cm column with pre-column, 10-μL injection, UV detection at 225 nm, solvent A: acetonitrile, solvent B: deionized water, 1 mL/min gradient as follows: Time (min:sec) % CH₃CN % H₂O 0:00 40 60 3:00 40 60 3:10 100 0 4:00 100 0 4:10 40 60 7:00 (stop) 40 60 Determination of Minimum Biocidal Concentration of Peracids

The method described by J. Gabrielson, et al. (J. Microbiol. Methods 50: 63-73 (2002)) was employed for determination of the Minimum Biocidal Concentration (MBC) of peracids, or for determination of the MBC of hydrogen peroxide and enzyme substrates. The assay method is based on XTT reduction inhibition, where XTT ((2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-5-[(phenylamino)carbonyl]-2H-tetrazolium, inner salt, monosodium salt) is a redox dye that indicates microbial respiratory activity by a change in optical density (OD) measured at 490 nm or 450 nm. However, there are a variety of other methods available for testing the activity of disinfectants and antiseptics including, but not limited to viable plate counts, direct microscopic counts, dry weight, turbidity measurements, absorbance, and bioluminescence (see, for example Brock, Semour S., Disinfection, Sterilization, and Preservation, 5^(th) edition, Lippincott Williams & Wilkins, Philadelphia, Pa., USA; 2001).

Determination of Virucidal Activity for Disinfectants and Antiseptics

Methods to evaluate the virucidal activity of disinfectants and antiseptics are well known in the art (Brock, S., supra and Papageorgiou et al., Appl. Environ. Microbiol., 67(12):5844-5848 (2001)). The present peracid compositions are expected to exhibit virucidal activity. It has been reported that acidic conditions (pH <7) may enhance virucidal activity. Accordingly, in a further aspect, the present peracid composition may be comprised of an acidic pH (pH <7). In another embodiment, the pH is less than 6.5, preferably less than 6, more preferably less than about 5.

Uses of Enzymatically Prepared Peracid Compositions

The enzyme-generated peracid produced according to the present methods can be used in a variety of applications for reduction of microbial, fungal, viral, and infectious protein (i.e., prion) contamination at a locus as defined herein, such as for the decontamination of medical instruments (e.g., endoscopes), textiles (e.g., garments, carpets), food preparation surfaces, food storage and food-packaging equipment, materials used for the packaging of food products, chicken hatcheries and grow-out facilities, animal enclosures, water treatment facilities, pools and spas, fermentation tanks, and spent process waters that have microbial and/or virucidal activity. In a preferred aspect, the present peracid compositions are particularly useful as a cleaning and disinfecting agent for non-autoclavable medical instruments and food packaging equipment. As the peracid-containing formulation may be prepared using GRAS or food-grade components (enzyme, enzyme substrate, hydrogen peroxide, and buffer), the enzyme-generated peracid may also be used for decontamination of animal carcasses, meat, fruits and vegetables, or for decontamination of prepared foods. The enzyme-generated peracid may be incorporated into a product whose final form is a powder, liquid, gel, solid or aerosol. The enzyme-generated peracid may be diluted to a concentration that still provides an efficacious decontamination.

The compositions comprising an efficacious concentration of peracid can be used to clean and disinfect surfaces and/or objects contaminated (or suspected of being contaminated) with pathogenic microorganisms, viruses, and/or prions by contacting the surface or object with the products produced by the present processes. As used herein, “contacting” refers to placing a disinfecting composition comprising an effective concentration of peracid in contact with a locus suspected of contamination with a disease-causing entity for a period of time sufficient to clean and disinfect. The time, temperature, and effective concentration used when contacting the desired locus can be easily determined by one of skill in the art. Contacting includes spraying, treating, immersing, flushing, pouring on or in, mixing, combining, painting, coating, applying, affixing to and otherwise communicating a peracid solution comprising an efficacious concentration of peracid with the surface or inanimate object suspected of being contaminated.

Peracid Disinfectants Having Prion-Degrading Activity

Patent applications PCT Publication No. WO 2004039418 A1, U.S. Patent Appln. Pub. No. 20020172989 A1, and co-filed US provisional patent application (D-Gen provisional patent application title) describe methods for the decontamination of prions that employ a protease or mixture of proteases to destroy the infectious prion protein (Langeveld et al., J. Infect. Diseases, 188:1782-1789 (2003)). The present examples also demonstrate that proteases capable of decontaminating infectious prions are capable of catalyzing the perhydrolysis of esters or amides to produce the corresponding peracid at concentrations efficacious for disinfection, thereby making possible the production of a mixture containing both an antimicrobial peracid and prion-degrading protease(s) using a single enzyme system.

Proteases for Biocidal Compositions Having Enhanced Prion-Degrading Activity

Enzymes cleaving the amide linkages in protein substrates are classified as proteases, or (interchangeably) peptidases (see Walsh, Enzymatic Reaction Mechanisms. W.H. Freeman and Company, San Francisco, Chapter 3 (1979) and Rao et al., Microbiol. Mol. Biol. Rev., 62(3):597-635 (1998)). It includes any enzyme belonging to the EC 3.4 enzyme group. These enzymes can be grossly subdivided into two major categories, exopeptidases and endopeptidases, depending upon their site of action.

As proteases are ubiquitous to all living organisms, suitable prion-degrading proteases can be isolated from a variety of eukaryotic and/or prokaryotic organisms. Commercially-useful proteases have been isolated from plants (e.g. papain, bromelain, and keratinases), animals (e.g., trypsin, pepsin, and rennin), and microbes such as fungi (e.g., Aspergillus oryzae proteases) and bacteria (especially well-known proteases isolated from the genus Bacillus). Bacillus species secrete two extracellular types of protease, neutral proteases (many of which are metallo-endoproteases, such as Neutrase®, typically active in a general pH range of 5 to 8) and alkaline proteases (such as Alcalase®, typically characterized by high activity at alkaline pH).

A sub-group of the serine proteases tentatively designated subtilases has been proposed by Siezen et al., supra. They are defined by homology analysis of more than 40 amino acid sequences of serine proteases previously referred to as subtilisin-like proteases. A subtilisin was previously defined as a serine protease produced by Gram-positive bacteria or fungi, and according to Siezen et al. now is a subgroup of the subtilases (or “subtilisin proteases”). A wide variety of subtilisins have been identified, and the amino acid sequence of a number of subtilisins have been determined. These include more than six subtilisins from Bacillus strains, namely, subtilisin 168, subtilisin BPN′, subtilisin Carlsberg, subtilisin Y, subtilisin amylosacchariticus, and mesentericopeptidase (Kurihara et al., J. Biol. Chem. 247 5629-5631 (1972); Wells et al., Nucleic Acids Res. 11 7911-7925 (1983); Stahl and Ferrari, J. Bacteriol. 159 811-819 (1984), Jacobs et al., Nucl. Acids Res. 13 8913-8926 (1985); Nedkov et al., Biol. Chem. Hoppe-Seyler 366 421-430 (1985), Svendsen et al., FEBS Lett. 196 228-232 (1986)), one subtilisin from an actinomycetales, thermitase from Thermoactinomyces vulgaris (Meloun et al., FEBS Lett. 198 195-200 (1985)), and one fungal subtilisin, Proteinase K from Tritirachium album (Jany and Mayer (1985) Biol. Chem. Hoppe-Seyler 366 584-492 (1985)). For further reference, see Table I from Siezen et al., supra.

Subtilisins are well-characterized physically and chemically. In addition to knowledge of the primary structure (amino acid sequence) of these enzymes, over 50 high resolution X-ray structures of subtilisins have been determined which delineate the binding of substrate, transition state, products, at least three different protease inhibitors, and define the structural consequences for natural variation (Kraut, Ann. Rev. Biochem. 46 331-358 (1977)).

One subgroup of the subtilases, I-S1, comprises the “classical” subtilisins, such as subtilisin 168, subtilisin BPN′, subtilisin Carlsberg (e.g., Alcalase®, available from Novozymes A/S, Bagsvaerd, Norway), and subtilisin DY.

A further subgroup of the subtilases I-S2, is recognized by Siezen et al. (supra). Sub-group I-S2 proteases are described as highly alkaline subtilisins and comprise enzymes such as subtilisin PB92 (e.g., Maxacal®), Gist-Brocades NV, Denmark), subtilisin 309 (e.g., Savinase®), Novozymes), subtilisin 147 (e.g., Esperase®), Novozymes), and alkaline elastase YaB.

Random and site-directed mutations of the subtilase gene have both arisen from knowledge of the physical and chemical properties of the enzyme and contributed information relating to subtilase's catalytic activity, substrate specificity, tertiary structure, etc. (Wells et al., Proc. Natl. Acad. Sci. U.S.A. 84:1219-1223 (1987); Wells et al., Phil. Trans. R. Soc. Lond.A. 317:415-423 (1986); Hwang and Warshel, Biochem. 26 2669-2673 (1987); Rao et al., Nature 328:551-554 (1987); Carter et al., Proteins 6:240-248 (1989); Graycar et al., Annals of the New York Academy of Sciences 672 71-79 (1992); and Takagi, Int. J. Biochem. 25 307-312 (1993).

Examples of proteases and protease variants have been disclosed in numerous United States patents and patent applications including, but not limited to U.S. patent application publications U.S. 200502391885 A1 and U.S. 20060147499 A1 and issued U.S. Patents: U.S. Pat. No. 5,500,364; U.S. Pat. No. 6,506,589; U.S. Pat. No. 6,555,355; U.S. Pat. No. 6,558,938; U.S. Pat. No. 6,558,939; U.S. Pat. No. 6,605,458; U.S. Pat. No. 6,632,646; U.S. Pat. No. 6,682,924; U.S. Pat. No. 6,773,907; U.S. Pat. No. 6,777,218; U.S. Pat. No. 6,780,629; U.S. Pat. No. 6,808,913; U.S. Pat. No. 6,835,821; U.S. Pat. No. 6,893,855; U.S. Pat. No. 6,921,657; U.S. Pat. No. 7,026,53; U.S. Pat. No. 7,098,017; and U.S. Pat. No. 7,109,016 (each hereby incorporated by reference in their entirety).

Examples of well-known, commercially-available proteases include, but are not limited to Pronase® (CAS # 9036-06-0; a protease mixture from Streptomyces griseus available from Calbiochem), Proteinase K (a fungal subtilisin from Tritirachium album), Alcalase® (Novozymes; also known as subtilisin Carlsberg or subtilisin A from Bacillus licheniformis; see GenBank® Accession No. P00780), Neutrasee (Novozymes; a neutral protease from Bacillus amyloliquefaciens; available from Sigma-Aldrich, catalog # P1236), Everlase® (Novozymes; a protease from Bacillus sp. available from Sigma-Aldrich, catalog #P5985), Polarzyme® (Novozymes; a protease engineered for low temperature washing applications), and Savinase® (Novozymes, also referred to as subtilisin 309 from Bacillus lentus; see GenBank® Accession No. P29600). The commercially-available enzymes may be incorporated into the present compositions and methods in a variety of product forms including powders, tablets, and liquid formulations. In another aspect, the commercially-available enzymes(s) may be optionally purified or partially purified prior to use in the present formulations. Means to purify proteins are well-known in the art.

Biocidal Compositions Comprising Prion-Degrading Proteases

Biocidal compositions comprising at least one prion-degrading protease and components suitable for in situ generation of a peracid are provided (i.e. a multifunctional biocidal composition comprising proteases to enhance prion degradation). In one aspect, the biocidal composition comprises a mixture of two or more prion-degrading proteases and components suitable for in situ generation of a peracid. In another aspect, one or more of the prion-degrading proteases also provides perhydrolysis activity for generating peracids from the present substrates.

In one embodiment, the present biocidal compositions includes components for in situ production (produced chemically and/or enzymatically) of at least one peracid. In a preferred embodiment, the peracid is primarily produced enzymatically from a suitable substrate as defined herein. In another preferred embodiment, the suitable substrate is a glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof. In another preferred aspect, the prion-degrading biocidal composition comprises in situ generated peracetic acid (and/or reaction components suitable for producing peracetic acid).

In another aspect, the present prion-degrading biocidal composition comprises at least one lipase and/or esterase having perhydrolysis activity for generating at least one peracid from the present substrates and at least one protease having prion-degrading activity. In a highly preferred aspect, the prion-degrading biocidal compositions comprise two or more proteases, wherein one or more of the proteases may also provide additional perhydrolysis activity.

In a preferred aspect, the source organism of the prion-degrading protease is selected from the group consisting of Bacillus subtilis, Bacillus amyloliquefaciens, Bacillus licheniformis, Bacillus lentus, Streptomyces griseus, and Tritirachium album. In a preferred embodiment, suitable prion-degrading proteases are selected from the group consisting of Alcalase® (available from Novozymes), Savinase® (available from Novozymes), Neutrase® (available from Novozymes), Polarzyme® (available from Novozymes), Everlase® (available from Novozymes), Streptomyces griseus Pronase (also known as Pronase E® or Pronase®; available from Calbiochem, La Jolla, Calif.), Tritirachium album Proteinase K (including recombinantly produced Proteinase K from Pichia pastoris), and mixtures thereof.

Combinations of several proteases have been identified as being particularly effective for enhancing prion degradation. In a preferred aspect, the biocidal composition comprises a mixture of Pronase® and Proteinase K and components suitable for in situ generation of a peracid. In another preferred aspect, a biocidal composition is provided comprising a mixture of Alcalase® and Neutrase® and components suitable for in situ generation of a peracid. In a further aspect, the biocidal composition comprises the above prion-degrading proteases and in situ generated peracid. In a preferred aspect, the in situ generated peracid is peracetic acid.

This composition comprising prion-degrading proteases and an efficacious concentration of a peracid may optionally include one or more surfactants and may include a period of heating to aid in prion decontamination. In one embodiment, the concentration of surfactant used when decontaminating prions may range from 0.01 to 50 wt %, preferably 0.1 to 10 wt %. The heat treatment step typically occurs at a temperature of at least 40° C. to 130° C., preferably at least 80° C., and most preferably at least 100° C. The optional heat treatment typically comprises a time of at least 1 minute up to 48 hours, preferably less than 24 hours, and most preferably less than 2 hours. In one embodiment, the method to degrade prions includes both a surfactant and a heat treatment. Additionally, the proteases may be used in combination with an added lipase at a pH where the protease(s) alone may not produce an efficacious concentration of peracid (e.g., at pH 4.0), the use of a synergistic combination of protease and lipase can produce a concentration of peracid greater than the sum of peracid produced by either protease or lipase alone.

The process to decontaminate a locus contaminated with (or at least suspected of being contaminated with) an infectious prion using the present aqueous peracid solutions may additionally include at least one step of treating the locus with a surfactant before or after contacting the locus with the aqueous peracid solution produced by the present process. In another embodiment, the surfactant may optionally be included in the peracid reaction mixture prior to contacting the prion contaminated locus. In yet another embodiment, the present process may optionally include a heat treatment step where the locus is heat treated before, during, or after contacting said locus with the aqueous peracid solution. In still yet another embodiment, the present process may include both the optional heating step and the surfactant treatment step.

General Methods

The following examples are provided to demonstrate preferred aspects of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

All reagents and materials were obtained from DIFCO Laboratories (Detroit, Mich.), GIBCO/BRL (Gaithersburg, Md.), TCI America (Portland, Oreg.), Charkit Chemical Corporation (Darien, Conn.), Eastman Chemical Co. (Kingsport, Tenn.) or Sigma/Aldrich Chemical Company (St. Louis, Mo.) unless otherwise specified. Enzymes were obtained from Sigma/Aldrich Chemical Company (St. Louis, Mo.), BioCatalytics (Pasadena, Calif.), Amano Enzymes USA (Lombard, Ill.), Valley Research (South Bend, Ind.), Enzyme Development Corporation (New York, N.Y.), and Novozymes (Franklinton, N.C.).

The abbreviations in the specification correspond to units of measure, techniques, properties, or compounds as follows: “sec” means second(s), “min” means minute(s), “h” or “hr” means hour(s), “d” means density in g/mL, “μL” means microliters, “mL” means milliliters, “L” means liters, “mM” means millimolar, “M” means molar, “mmol” means millimole(s), “wt” means weight, “wt %” means weight percent, “g” means grams, “μg” means micrograms, HPLC” means high performance liquid chromatography, “O.D.” means optical density at the designated wavelength, “dcw” means dry cell weight, “CFU” means colony forming units, “ATCC” means American Type Culture Collection, “U” means units of perhydrolase activity, “RPM” means revolutions per minute, “EDTA” means ethylenediaminetetraacetic acid, “dd” means distilled and deionized, and “DTT” means dithiothreitol.

EXAMPLE 1 Lipase-Catalyzed Perhydrolysis of Triacetin at pH 6.5

Into a 4-mL glass vial with stir bar was added 1 mg enzyme (ICR 101-117, BioCatalytics, Pasadena, Calif.) in 0.050 mL of 50 mM potassium phosphate buffer (pH 6.5), 0.900 mL of 278 mM triacetin in 50 mM potassium phosphate buffer (pH 6.5, 250 mM final triacetin concentration), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 Nominal Molecular Weight Limit (NMWL) filter (Millipore UltraFree-MC, Millipore Corp., Billerica, Mass.) centrifuged for2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 1). TABLE 1 Lipase-catalyzed Perhydrolysis of 250 mM Triacetin at pH 6.5. peracetic acid peracetic acid enzyme enzyme source (ppm), 5 min (ppm), 30 min ICR-101 Aspergillus sp. 282 179 ICR-102 Rhizopus sp. 80 235 ICR-103 Rhizopus oryzae 113 36 ICR-104 Penicillium sp. I 131 142 ICR-105 Penicillium sp. II 144 66 ICR-106 Candida rugosa 171 105 ICR-107 Pseudomonas cepacia 179 0 ICR-108 Pseudomonas sp. 180 30 ICR-109 Pseudomonas fluorescens 183 11 ICR-110 Candida antartica lipase B 337 398 ICR-111 Candida sp. 238 117 ICR-112 Candida antartica lipase A 134 0 ICR-113 Pseudomonas sp. 241 358 ICR-114 porcine pancreas 135 0 ICR-115 T. languinosus 216 113 ICR-116 Mucor miehei 238 117 ICR-117 Alcaligenes sp. 293 370

EXAMPLE 2 Lipase-Catalyzed Perhydrolysis of Triacetin at pH 4.0

Into a 4-mL glass vial with stir bar was added 1 mg enzyme (ICR 101 -117, BioCatalytics, Pasadena, Calif.) in 0.050 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0), 0.900 mL of 278 mM triacetin in 50 mM sodium acetate/acetic acid buffer (pH 4.0, 250 mM final triacetin concentration), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 2). TABLE 2 Lipase-catalyzed Perhydrolysis of 250 mM Triacetin at pH 4.0. peracetic acid peracetic acid enzyme enzyme source (ppm), 5 min (ppm), 30 min no enzyme 10 9.6 ICR-101 Aspergillus sp. 238 555 ICR-102 Rhizopus sp. 11 0 ICR-103 Rhizopus oryzae 0 4 ICR-104 Penicillium sp. I 9 16 ICR-105 Penicillium sp. II 11 19 ICR-106 Candida rugosa 23 34 ICR-107 Pseudomonas cepacia 32 135 ICR-108 Pseudomonas sp. 33 53 ICR-109 Pseudomonas fluorescens 32 68 ICR-110 Candida antartica lipase B 362 688 ICR-111 Candida sp. 24 79 ICR-112 Candida antartica lipase A 151 86 ICR-113 Pseudomonas sp. 221 370 ICR-114 porcine pancreas 165 53 ICR-115 T. languinosus 206 132 ICR-116 Mucor miehei 14 0 ICR-117 Alcaligenes sp. 185 710

EXAMPLE 3 Lipase-Catalyzed Perhydrolysis of Triacetin at pH 4.0

Into a 4-mL glass vial with stir bar was added 2 mg enzyme (lipase ICR 101 or ICR 110, BioCatalytics, Pasadena, Calif.) and 1.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) containing from 250 mM or 500 mM triacetin and 500 mM or 2500 mM hydrogen peroxide). After stirring for 5 or 30 minutes at 23° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:20 with dd water and analyzed for peracid using the HPLC assay method (Table 3). TABLE 3 Lipase-catalyzed Perhydrolysis of 250 mM or 500 mM Triacetin at pH 4.0. triacetin H₂O₂ peracetic acid peracetic acid enzyme (mM) (mM) (ppm), 5 min (ppm), 30 min no enzyme 250 500 10 10 ICR-101 250 500 461 1030 ICR-110 250 500 498 568 no enzyme 250 2500 17 15 ICR-101 250 2500 656 1158 ICR-110 250 2500 1570 2880 no enzyme 500 2500 10 207 ICR-101 500 2500 612 1109 ICR-110 500 2500 1860 3755

EXAMPLE 4 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 6.5

Into a 4-mL glass vial with stir bar was added 1 mg enzyme (ICR 101 -117, BioCatalytics, Pasadena, Calif.) in 0.050 mL of 50 mM potassium phosphate buffer (pH 6.5), 0.900 mL of an aqueous mixture containing diacetin (278 mM), triacetin (144 mM) and monoacetin (131 mM) in 50 mM potassium phosphate buffer (pH 6.5), and either 0.052 mL 30% hydrogen peroxide (500 mM final concentration) or 0.026 mL 30% hydrogen peroxide (250 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 4). TABLE 4 Lipase-catalyzed Perhydrolysis of a Mixture of Diacetin (278 mM), Triacetin (144 mM) and Monoacetin (131 mM) at pH 6.5. 250 mM 250 mM 500 mM 500 mM H₂O₂ H₂O₂ H₂O₂ H₂O₂ peracetic peracetic peracetic peracetic acid acid acid acid enzyme (ppm), 5 min (ppm), 30 min (ppm), 5 min (ppm), 30 min no enzyme 16 56 19 44 ICR-101 136 250 194 277 ICR-102 127 159 26 232 ICR-103 139 133 275 223 ICR-104 151 174 284 286 ICR-105 0 0 0 0 ICR-106 0 16 29 47 ICR-107 0 102 17 54 ICR-108 3 27 0 7 ICR-109 0 38 38 0 ICR-110 451 384 669 484 ICR-111 0 21 12 43 ICR-112 0 24 20 38 ICR-113 34 202 80 236 ICR-114 0 0 0 0 ICR-115 0 8 11 8 ICR-116 0 7 0 0 ICR-117 114 353 61 456

EXAMPLE 5 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 4.0

Into a 4-mL glass vial with stir bar was added 1 mg enzyme (ICR 101, 110, 113, or 117, BioCatalytics, Pasadena, Calif.) in 0.050 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0), 0.900 mL of an aqueous mixture containing either a) diacetin (278 mM), triacetin (144 mM) and monoacetin (131 mM) in 50 mM sodium acetate/acetic acid buffer (pH 4.0) or b) diacetin (131 mM), triacetin (68 mM) and monoacetin (62 mM) in 50 mM sodium acetate/acetic acid buffer (pH 4.0), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 5). TABLE 5 Lipase-catalyzed Perhydrolysis of Mixtures of Diacetin, Triacetin and Monoacetin at pH 4.0. diacetin diacetin (131 mM), (278 mM), triacetin triacetin (68 mM), (144 mM) monoacetin monoacetin substrate (62 mM) (131 mM) concen- peracetic peracetic peracetic peracetic tration acid acid acid acid enzyme (ppm), 5 min (ppm), 30 min (ppm), 5 min (ppm), 30 min no enzyme 4 2 1 2 ICR-101 183 457 ICR-110 502 616 982 948 ICR-113 102 358 ICR-117 280 896

EXAMPLE 6 Protease-Catalyzed Perhydrolysis of Acetamide and Diacetamide at pH 4.0

Into a 4-mL glass vial with stir bar was added 1 mg protease (Table 6) in 0.050 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0), 0.900 mL of an aqueous mixture containing either a) acetamide (278 mM) in 50 mM sodium acetate/acetic acid buffer (pH 4.0) or b) diacetamide (278 mM) in 50 mM sodium acetate/acetic acid buffer (pH 4.0), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 7). TABLE 6 Protease and Supplier. catalog enzyme, source number supplier Protease Type XIII, Aspergillus saitoi P2143 Sigma Protease Type XVIII, Rhizopus sp. P5027 Sigma Protease, Bacillus sp. P5985 Sigma Pepsin, porcine stomach P6887 Sigma Chymopapain, papaya latex C8526 Sigma Bromelain, pineapple stem 3000 GDU Hong Mao Biochemicals Papain, papaya latex P3125 Sigma Pronase, S. griseus 81748 Biochemika Proteinase K, T. album, 3115879 Roche recombinantly expressed in P. pastoris Proteinase K, T. album 70663 Novagen

TABLE 7 Protease-catalyzed Perhydrolysis of Acetamide (250 mM) and Diacetamide (250 mM) at pH 4.0. acetamide acetamide diacetamide diacetamide (250 mM) (250 mM) (250 mM) (250 mM) peracetic acid peracetic acid peracetic acid peracetic acid protease (ppm), 5 min (ppm), 30 min (ppm), 5 min (ppm), 30 min no enzyme (control) 0 0 4 16 Protease Type XIII 35 49 88 116 Protease Type XVIII 27 41 94 107 Protease, Bacillus sp. 48 61 95 138 Pepsin 45 65 97 120 Chymopapain 66 65 100 131 Bromelain 57 63 92 130 Papain 81 105 135 172 Pronase 2 43 Proteinase K, T. album, 26 43 recombinantly expressed in P. pastoris Proteinase K, T. album 34 49

EXAMPLE 7 Protease-Catalyzed Perhydrolysis of Triacetin at pH 4.0

Into a 4-mL glass vial with stir bar was added 1 mg protease (Table 6) in 0.050 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0), 0.900 mL of an aqueous mixture containing triacetin (278 mM) in 50 mM sodium acetate/acetic acid buffer (pH 4.0), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 8). TABLE 8 Protease-catalyzed Perhydrolysis of Triacetin (250 mM) at pH 4.0. triacetin triacetin (250 mM) (250 mM) peracetic acid peracetic acid protease (ppm), 5 min (ppm), 30 min no enzyme (control) 10 10 Protease Type XIII 209 358 Protease Type XVIII 65 30 Protease, Bacillus sp. 74 55 Pepsin 65 44 Chymopapain 72 57 Bromelain 83 59 Papain 85 48

EXAMPLE 8 Protease-Catalyzed Perhydrolysis of Triacetin at pH 6.5

Into a 4-mL glass vial with stir bar was added 1 mg protease (Table 6) in 0.050 mL of 50 mM sodium phosphate buffer (pH 6.5), 0.900 mL of an aqueous mixture containing triacetin (278 mM) in 50 mM phosphate buffer (pH 6.5), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 9). TABLE 9 Protease-catalyzed Perhydrolysis of Triacetin (250 mM) at pH 6.5. triacetin triacetin (250 mM) (250 mM) peracetic acid peracetic acid protease (ppm), 5 min (ppm), 30 min no enzyme (control) 51 26 Protease Type XIII 135 136 Protease Type XVIII 89 119 Protease, Bacillus sp. 93 64 Pepsin 111 163 Chymopapain 69 167 Bromelain 161 170 Papain 203 142

EXAMPLE 9 Protease-Catalyzed Perhydrolysis of Acetamide and Diacetamide at pH 6.5

Into a 4-mL glass vial with stir bar was added 1 mg protease (Table 6) in 0.050 mL of 50 mM potassium phosphate buffer (pH 6.5), 0.900 mL of an aqueous mixture containing either a) acetamide (278 mM) in 50 mM potassium phosphate buffer (pH 6.5) or b) diacetamide (278 mM) in 50 mM potassium phosphate buffer (pH 6.5), and 0.052 mL 30% hydrogen peroxide (500 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 10). TABLE 10 Protease-catalyzed Perhydrolysis of Acetamide (250 mM) and Diacetamide (250 mM) at pH 6.5. acetamide acetamide diacetamide diacetamide (250 mM) (250 mM) (250 mM) (250 mM) peracetic acid peracetic acid peracetic acid peracetic acid protease (ppm), 5 min (ppm), 30 min (ppm), 5 min (ppm), 30 min no enzyme (control) 23 26 59 62 Pronase 126 168 17 17 Proteinase K, T. album, 150 194 66 99 recombinantly expressed in P. pastoris Proteinase K, T. album 270 214 104 100 no enzyme (control) 21 0 0 33 Protease Type XIII 42 32 218 206 Protease Type XVIII 58 33 226 180 Protease, Bacillus sp. 89 73 807 181 Pepsin 81 67 259 198 Chymopapain 94 12 218 170 Bromelain 108 112 311 202 Papain 199 157 342 187

EXAMPLE 10 Enzymatic Perhydrolysis of Triacetin Using a Combination of Lipase and Proteases at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (ICR 101, ICR-110, or ICR-1 17, BioCatalytics, Pasadena, Calif.), 0.3 mg Proteinase K (T. album), and 1.2 mg of Pronase in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing triacetin (250 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) 20 centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 11). Reactions were also run with lipase alone or protease(s) alone for comparison of peracetic acid concentrations produced without the combination of lipase and protease(s). TABLE 11 Enzymatic Perhydrolysis of Triacetin (250 mM) using a Combination of Lipase and Proteases at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 10 10 Proteinase K 4.0 24 7 Pronase 4.0 17 5 Proteinase K/Pronase 4.0 8 15 ICR-101 4.0 238 555 Proteinase K/Pronase/ICR101 4.0 252 542 ICR-110 4.0 362 688 Proteinase K/Pronase/ICR110 4.0 460 679 ICR-117 4.0 284 927 Proteinase K/Pronase/ICR117 4.0 401 909 no enzyme (control) 6.5 22 59 Proteinase K 6.5 323 669 Pronase 6.5 114 484 Proteinase K/Pronase 6.5 225 433 ICR-101 6.5 306 588 Proteinase K/Pronase/ICR101 6.5 359 576 ICR-110 6.5 337 398 Proteinase K/Pronase/ICR110 6.5 406 364 ICR-117 6.5 438 984 Proteinase K/Pronase/ICR117 6.5 579 1189

EXAMPLE 11 (COMPARATIVE) Enzymatic Perhydrolysis of Propyl Acetate or Triacetin at pH 6.5

Into a 4-mL glass vial with stir bar was added 2 mg of one of the following enzymes: acetylcholinesterase (Sigma, C-2888), Lipase G “Amano”50 (Amano), or Chirazyme L2, lyo. (C. antartica lipase B, BioCatalytics) dissolved in 0.050 mL of 50 mM potassium phosphate buffer (pH 6.5). To the vial was then added either a) 0.930 mL of a solution containing 50 mM potassium phosphate buffer (pH 6.5) and 215 mM propyl acetate, followed by 0.021 mL 30% hydrogen peroxide (200 mM final hydrogen peroxide concentration) or b) 0.900 mL of a solution containing 278 mM triacetin in 50 mM potassium phosphate buffer (pH 6.5), 0.024 mL of 50 mM potassium phosphate buffer (pH 6.5), and 0.026 mL 30% hydrogen peroxide (250 mM final concentration). After stirring for 5 or 30 minutes at 22° C., a 0.250 mL sample of the reaction mixture was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the resulting filtrate was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the filtrate was directly analyzed for peracid using the HPLC assay method (Table 12). TABLE 12 Enzymatic Perhydrolysis of Propyl Acetate (200 mM) or Triacetin (250 mM) at pH 6.5. propyl acetate propyl acetate triacetin triacetin (200 mM), (200 mM), (250 mM), (250 mM) H₂O₂ H₂O₂ H₂O₂ H₂O₂ (200 mM) (200 mM) (250 mM) (250 mM) peracetic acid peracetic acid peracetic acid peracetic acid enzyme (ppm), 5 min (ppm), 30 min (ppm), 5 min (ppm), 30 min no enzyme (control) 12 69 22 70 acetyl cholinesterase 0 0 Lipase G “Amano” 50 18 46 78 Chirazyme L2 19 1 192 173

EXAMPLE 12 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 6.5

A 1-mL reaction mixture was prepared containing 2 mg, 1 mg or 0.2 mg of enzyme (A“Amano”12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), ICR 110 (C. antartica lipase, BioCatalytics), Dietrenz CR (C. rugosa lipase, Valley Research), Amano F-DS (R. oryzae lipase, Amano), Amano DS (A. niger lipase, Amano), or Enzeco MLC (Microbial Lipase Concentrate, A. niger lipase, Enzyme Development Corporation)) dissolved in 1.0 mL of 50 mM potassium phosphate buffer (pH 6.5) containing a mixture of diacetin (236 mM), triacetin (83 mM) and monoacetin (181 mM) and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 13). TABLE 13 Lipase-catalyzed Perhydrolysis of Diacetin (236 mM), Triacetin (83 mM) and Monoacetin (181 mM) at pH 6.5. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 80 60 A“Amano”12 2 2500 460 520 Validase AN 2 2500 590 510 ICR-110 2 2500 2290 2350 A“Amano”12 1 2500 420 350 Validase AN 1 2500 190 390 ICR-110 1 2500 2100 2240 ICR-110 0.2 2500 610 1850 no enzyme 0 1000 90 110 A“Amano”12 2 1000 310 580 Validase AN 2 1000 340 550 ICR-110 2 1000 1240 1030 A“Amano”12 1 1000 240 525 Validase AN 1 1000 220 470 ICR-110 1 1000 335 595 Dietrenz CR 1 1000 70 240 Amano F-DS 1 1000 10 10 Amano DS 1 1000 170 430 Enzeco MLC 1 1000 155 390 ICR-110 0.2 1000 380 410 no enzyme 0 500 40 30 A“Amano”12 1 500 215 490 Validase AN 1 500 120 500 ICR-110 1 500 240 490 Dietrenz CR 1 500 0 210 Amano F-DS 1 500 35 75 Amano DS 1 500 60 305 Enzeco MLC 1 500 145 405

EXAMPLE 13 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 4.0

A 1-mL reaction mixture was prepared containing 2 mg, 1 mg or 0.2 mg of enzyme (A“Amano”12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), or ICR 110 (C. antartica lipase, BioCatalytics)) dissolved in 1.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) containing a mixture of diacetin (236 mM), triacetin (83 mM) and monoacetin (181 mM) and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 14). TABLE 14 Lipase-catalyzed Perhydrolysis of Diacetin (236 mM), Triacetin (83 mM) and Monoacetin (181 mM) at pH 4.0. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 10 40 A“Amano”12 2 2500 870 605 Validase AN 2 2500 510 560 ICR-110 2 2500 1670 2250 A“Amano”12 1 2500 240 700 Validase AN 1 2500 270 600 ICR-110 1 2500 1740 2180 ICR-110 0.2 2500 480 1470 no enzyme 0 1000 10 10 A“Amano”12 2 1000 320 600 Validase AN 2 1000 270 690 ICR-110 2 1000 1080 920 ICR-110 0.2 1000 870 1060

EXAMPLE 14 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 6.5

A 1-mL reaction mixture was prepared containing 2 mg or 1 mg of enzyme (A“Amano”12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), or ICR 110 (C. antartica lipase, BioCatalytics)) dissolved in 1.0 mL of 50 mM potassium phosphate buffer (pH 6.5) containing a mixture of diacetin (500 mM), triacetin (176 mM) and monoacetin (383 mM), and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 15). TABLE 15 Lipase-catalyzed Perhydrolysis of a Mixture of Diacetin (500 mM), Triacetin (176 mM) and Monoacetin (383 mM) at pH 6.5. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 11 13 A″Amano″12 2 2500 394 860 Validase AN 2 2500 354 650 ICR-110 2 2500 5224 7130 A″Amano″12 1 2500 290 710 Validase AN 1 2500 220 450 ICR-110 1 2500 3290 6130 no enzyme 0 1000 70 50 A″Amano″12 2 1000 420 930 Validase AN 2 1000 490 890 ICR-110 2 1000 2900 2600

EXAMPLE 15 Lipase-Catalyzed Perhydrolysis of a Mixture of Diacetin, Triacetin and Monoacetin at pH 4.0

A 1-mL reaction mixture was prepared containing 2 mg or 1 mg of enzyme (A“Amano”12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), or ICR 110 (C. antartica lipase, BioCatalytics)) dissolved in 1.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) containing a mixture of diacetin (500 mM), triacetin (176 mM) and monoacetin (383 mM), and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 16). TABLE 16 Lipase-catalyzed Perhydrolysis of a mixture of Diacetin (500 mM), Triacetin (176 mM) and Monoacetin (383 mM) at pH 4.0. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 10 10 A″Amano″12 2 2500 380 920 Validase AN 2 2500 440 930 ICR-110 2 2500 5760 7210 A″Amano″12 1 2500 180 480 Validase AN 1 2500 170 520 ICR-110 1 2500 3960 7450 no enzyme 0 1000 10 10 A″Amano″12 2 1000 380 900 Validase AN 2 1000 400 1150 ICR-110 2 1000 2970 2510

EXAMPLE 16 Lipase-Catalyzed Perhydrolysis of Triacetin at pH 6.5

A 1-mL reaction mixture was prepared containing 2 mg, 1 mg or 0.2 mg of enzyme (A“Amano”12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), and ICR 110 (C. antartica lipase, BioCatalytics)) dissolved in 1.0 mL of 50 mM potassium phosphate buffer (pH 6.5) containing 500 mM triacetin and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 17). TABLE 17 Lipase-catalyzed Perhydrolysis of Triacetin (500 mM) at pH 6.5. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 80 170 A″Amano″12 2 2500 800 1390 Validase AN 2 2500 790 1180 ICR-110 2 2500 2710 2880 A″Amano″12 1 2500 670 1070 Validase AN 1 2500 460 810 ICR-110 1 2500 1840 2421 ICR-110 0.2 2500 1120 760 no enzyme 0 1000 130 80 A″Amano″12 2 1000 970 1250 Validase AN 2 1000 770 1310 ICR-110 2 1000 760 1400 ICR-110 0.2 1000 450 680

EXAMPLE 17 Lipase-Catalyzed Perhydrolysis of Triacetin at pH 4.0

A 1-mL reaction mixture was prepared containing 2 mg, 1 mg or 0.2 mg of enzyme (A“Amano” 12 lipase (A. niger lipase, Amano), Validase lipase AN (A. niger lipase, Valley Research), or ICR 110 (C. antartica lipase, BioCatalytics)) dissolved in 1.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) containing triacetin (500 mM) and either 2500 mM or 1000 mM hydrogen peroxide. After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:25 with dd water and analyzed for peracid using the HPLC assay method (Table 18). TABLE 18 Lipase-catalyzed Perhydrolysis of Triacetin (500 mM) at pH 4.0. [enzyme] H₂O₂ peracetic acid peracetic acid enzyme (mg/mL) (mM) (ppm), 5 min (ppm), 30 min no enzyme 0 2500 10 20 A″Amano″12 2 2500 1030 1370 Validase AN 2 2500 920 840 ICR-110 2 2500 2810 3700 A″Amano″12 1 2500 570 740 Validase AN 1 2500 570 680 ICR-110 1 2500 2120 2860 ICR-110 0.2 2500 510 780 no enzyme 0 1000 5 5 A″Amano″12 2 1000 1100 1520 Validase AN 2 1000 930 1230 ICR-110 2 1000 1540 1670 ICR-110 0.2 1000 370 600

EXAMPLE 18 CALB L-Catalyzed Perhydrolysis of Triacetin at pH 4.0 and pH 6.5

A 1-mL reaction mixture was prepared containing 0.010 mL of CALB L lipase (a commercial liquid formulation of C. antartica lipase B, Novozymes) dissolved in either 1.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) or 1.0 mL of 50 mM potassium phosphate buffer (pH 6.5) additionally containing triacetin (250 mM) and hydrogen peroxide (2500 mM). After stirring for 5 or 30 minutes at 25° C., a 0.250 mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:20 with dd water and analyzed for peracid using the HPLC assay method (Table 19). TABLE 19 Lipase-catalyzed Perhydrolysis of Triacetin (250 mM) at pH 4.0 or pH 6.5 using CALB L. H₂O₂ peracetic acid peracetic acid enzyme pH (mM) (ppm), 5 min (ppm), 30 min no enzyme 4.0 2500 28 15 CALB L 4.0 2500 439 1120 no enzyme 6.5 2500 226 108 CALB L 6.5 2500 1294 678

EXAMPLE 19 Perhydrolysis of Triacetin at pH 4.0 using Immobilized C. antartica Lipase B

A reaction mixture was prepared containing 100 mg of IMB-111 (immobilized Candida antartica lipase B, BioCatalytics) suspended in 10.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0) additionally containing triacetin (500 mM) and hydrogen peroxide (2500 mM). After mixing on a rotating platform for a predetermined time from 2 to 30 minutes at 25° C., a 0.100 mL sample of the liquid portion was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:20 with dd water and analyzed for peracid using the HPLC assay method (Table 20). TABLE 20 Lipase-catalyzed Perhydrolysis of Triacetin (500 mM) at pH 4.0 using immobilized Candida Antartica lipase B (IMB-111). no enzyme, 10 mg/mL IMB-111, Time peracetic acid peracetic acid (min) (ppm) (ppm)  2 42 911  5 50 1667 10 49 2244 15 24 2755 20 43 3261 25 49 3369 30 57 3757

The above reaction was repeated with fresh catalyst, and after 30 min, the concentration of peracetic acid was 3621 ppm. The catalyst was recovered from the reaction mixture, washed twice with 10.0 mL of 50 mM sodium acetate/acetic acid buffer (pH 4.0), and the reaction was repeated using the recovered enzyme; after 30 min, the concentration of peracetic acid was 2274 ppm.

EXAMPLE 20 Timecourse for Enzymatic Perhydrolysis of Triacetin at pH 6.5

A reaction mixture containing 1.0 mg/mL of DS lipase (A. niger, Amano) dissolved in 50 mM potassium phosphate buffer (pH 6.5) containing hydrogen peroxide (2500 mM) and triacetin (500 mM) was stirred at 25° C. A 0.100 mL aliquot was withdrawn at pre-determined times and filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) for 2 minute at 12,000 RPM. A portion of the filtered reaction sample was diluted 1:20 with dd water and analyzed for peracid using the HPLC assay method (Table 21). TABLE 21 Timecourse for DS Lipase-catalyzed Perhydrolysis of Triacetin (500 mM) at pH 6.5. no enzyme, 1 mg/mL DS lipase, Time peracetic acid peracetic acid (min or h) (ppm) (ppm) 5 min 10 367 30 min 149 522 2 h 26 819 5 h 78 1481 19 h 27 1895

EXAMPLE 21 Biocidal Activity of a Peracetic Acid Formulation Prepared from Triacetin, Hydrogen Peroxide and C. antartica Lipase B

A reaction was performed using Chirazyme L2 lipase (C. antartica lipase B) as enzyme catalyst for the production of peracetic acid. Into a 20-mL glass vial equipped with magnetic stir bar was placed 9.00 mL of 278 mM triacetin in 50 mM phosphate buffer (pH 6.5), 0.258 mL of 30% hydrogen peroxide, and 1.0 mL of 20 mg/mL Chirazyme L2 in 50 mM phosphate buffer (pH 6.5), and the resulting mixture stirred for 5 min at room temperature. The reaction was stopped by filtering the product mixture using a 30K NMWL filter unit (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 rpm to remove the enzyme, and storing the filtrate on wet ice. The filtrate was analyzed for peracetic acid (PM) and hydrogen peroxide using the HPLC assay method; control reactions were performed in the absence of added enzyme with and without triacetin. The filtered enzyme-generated product mixture contained 192 ppm PM, produced from both the chemical and enzymatic reaction of triacetin with hydrogen peroxide; the hydrogen peroxide concentration in the product mixture was 6431 ppm. The control reaction performed with 250-mM triacetin and no added enzyme produced 22 ppm PM generated from the chemical reaction of triacetin and hydrogen peroxide.

The filtered enzyme-generated product mixture was diluted 1:5 with sterile water, and the resulting solution was further diluted with sterile water in four 1:1 serial dilutions to obtain the concentrations of PM and hydrogen peroxide listed in Table 22. TABLE 22 Dilution Series Used to Assessing Biocidal Activity. dilution factor PAA (ppm) H₂O₂ (ppm) 1:5  38.3 1286 1:10 19.2 643 1:20 9.6 322 1:40 4.8 161 1:80 2.4 80

The 1:5 dilution and four serial dilutions were evaluated for biocidal activity by mixing 0.100 mL of the PM-containing solution with 0.100 mL of an inoculum containing 2.7×10⁶ CFU/mL of E. Coli ATCC 11229 (American Type Culture Collection, Manassas, Va.) in Millers LB broth diluted with Butterfield Buffer; eight replicates of each mixture were contained in individual wells of a sterile 96-well microtiter plate. After the resulting cell suspensions were allowed to stand for 10 minutes at room temperature, they were tested for viability using the growth indicator XTT (2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-5-[(phenylamino)carbonyl]-2H-tetrazolium, inner salt, monosodium salt; CAS RN 111072-31-2) according to the method of Gabrielson et al. (J. Microbiol. Methods, 50:63-73 (2002)). No cell growth of 1.35×10⁶ CFU/mL (indicated by no OD measurement at 450 nm using XTT) was observed with a Minimum Biocidal Concentration of PAA of 2.4 ppm (six-log kill) (Table 23). TABLE 23 Determination of Minimum Biocidal Concentration (MBC) of Peracetic Acid Generated by Lipase-catalyzed Perhydrolysis of Triacetin for E. coli ATCC 11229. PAA (ppm) 19.15 9.6 4.8 2.4 1.2 control H₂O₂ (ppm) 0 643.1 321.6 160.8 80.4 40.2 0 blank replicate 1 OD (450 nm) 0.403 0.427 0.418 0.406 0.692 2.177 0.418 replicate 2 OD (450 nm) 0.383 0.398 0.393 0.400 0.674 2.142 0.415 replicate 3 OD (450 nm) 0.379 0.392 0.388 0.397 0.635 2.007 0.414 replicate 4 OD (450 nm) 0.387 0.395 0.399 0.403 0.658 2.114 0.418 replicate 5 OD (450 nm) 0.381 0.404 0.398 0.401 0.625 2.171 0.409 replicate 6 OD (450 nm) 0.382 0.409 0.404 0.409 0.639 2.347 0.405 replicate 7 OD (450 nm) 0.382 0.394 0.401 0.407 0.520 2.323 0.407 replicate 8 OD (450 nm) 0.403 0.422 0.471 0.543 0.496 2.582 0.428 mean replicate OD (450 nm) 0.388 0.405 0.409 0.421 0.617 2.233 0.414 blank-corrected mean −0.029 −0.009 −0.005 0.007 0.203 1.819 0 OD:

Separately, the cell inoculum was treated with sterile solutions of triacetin (Table 24) or hydrogen peroxide in 50 mM phosphate buffer (pH 6.5) (Table 25) at the concentrations present in each of the biocide dilutions in Table 23 to determine the MBC for these components of the biocide solution. TABLE 24 Determination of Minimum Biocidal Concentration (MBC) of Triacetin for E. coli ATCC 11229. triacetin (ppm) 5455 2728 1364 682 341 control 0 blank replicate 1 OD (450 nm) 2.210 2.280 2.337 2.213 2.408 2.375 0.401 replicate 2 OD (450 nm) 2.136 2.208 2.265 2.156 2.507 2.397 0.420 replicate 3 OD (450 nm) 2.091 2.222 2.198 2.218 2.189 2.386 0.402 replicate 4 OD (450 nm) 2.229 2.273 2.140 2.304 2.568 2.557 0.409 replicate 5 OD (450 nm) 2.124 2.167 2.266 2.310 2.563 2.491 0.413 replicate 6 OD (450 nm) 2.263 2.358 2.485 2.560 2.601 2.582 0.410 replicate 7 OD (450 nm) 2.407 2.454 2.632 2.601 2.58 2.603 0.410 replicate 8 OD (450 nm) 2.539 2.663 2.823 2.605 3.148 2.952 0.455 mean replicate OD (450 nm) 2.250 2.328 2.393 2.371 2.571 2.543 0.415 blank-corrected mean OD: 1.835 1.913 1.978 1.956 2.156 2.128 0

TABLE 25 Determination of Minimum Biocidal Concentration (MBC) of Hydrogen Peroxide for E. coli ATCC 11229. H₂0₂ (ppm) 680.5 340.2 170.1 85.1 42.5 control 0 blank replicate 1 OD (450 nm) 0.456 0.440 0.401 1.880 2.170 2.371 0.423 replicate 2 OD (450 nm) 0.436 0.428 0.422 1.793 2.082 2.226 0.417 replicate 3 OD (450 nm) 0.446 0.424 0.470 1.834 2.034 2.158 0.415 replicate 4 OD (450 nm) 0.433 0.423 0.435 1.889 2.007 2.216 0.422 replicate 5 OD (450 nm) 0.440 0.439 0.402 1.815 2.027 2.372 0.417 replicate 6 OD (450 nm) 0.426 0.425 0.424 1.795 1.971 2.581 0.419 replicate 7 OD (450 nm) 0.430 0.432 0.462 1.962 2.117 2.741 0.442 replicate 8 OD (450 nm) 0.453 0.452 0.414 2.153 2.666 2.821 0.439 mean replicate OD (450 nm) 0.440 0.433 0.4295 1.890 2.134 2.436 0.424 blank-corrected mean OD: 0.016 0.009 0.005 1.466 1.710 2.012 0

The MBC of PM for E. coil ATCC 11229 was >2.4 ppm, measured in the presence of 80 ppm of hydrogen peroxide (Table 23); the MBC for hydrogen peroxide was >170 ppm (Table 25), confirming that the biocidal activity of the PAA test solution was due to PAA and not H₂O₂. Triacetin had no biocidal effect at the highest concentration examined (5455 ppm, Table 24). The MBC for PAA generated enzymatically agrees closely with the MBC determined using a commercial source of peracetic acid (Table 26, MBC >2.3 ppm PAA). TABLE 26 Determination of Minimum Biocidal Concentration (MBC) of Commercially-Available Peracetic Acid for E. coli ATCC 11229. PAA (ppm) 18.75 9.4 4.7 2.3 1.15 control 0 blank replicate 1 OD (450 nm) 0.306 0.301 0.310 0.303 1.734 2.098 0.305 replicate 2 OD (450 nm) 0.292 0.296 0.297 0.288 1.367 1.832 0.295 replicate 3 OD (450 nm) 0.289 0.290 0.294 0.292 1.343 1.816 0.295 replicate 4 OD (450 nm) 0.288 0.294 0.295 0.291 1.377 1.874 0.292 replicate 5 OD (450 nm) 0.296 0.291 0.298 0.294 1.368 1.869 0.294 replicate 6 OD (450 nm) 0.294 0.294 0.294 0.292 1.378 1.874 0.290 replicate 7 OD (450 nm) 0.296 0.299 0.293 0.303 1.324 1.817 0.227 replicate 8 OD (450 nm) 0.300 0.295 0.304 0.318 1.386 1.869 0.173 mean replicate OD (450 nm) 0.295 0.295 0.298 0.298 1.410 1.881 0.271 blank-corrected mean OD: 0.024 0.024 0.027 0.026 1.138 1.610 0

EXAMPLE 22 Enzymatic Perhydrolysis of Triacetin using a Combination of Lipase and Alcalase® at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-11 0 (BioCatalytics)), and 20 μL Alcalase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing triacetin (250 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 27). Reactions were also run with lipase alone or Alcalase® alone for comparison of peracetic acid concentrations produced without the combination of lipase and Alcalase®. TABLE 27 Enzymatic Perhydrolysis of Triacetin (250 mM) Using a Combination of Lipase and Alcalase ® at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 10 10 Alcalase ® 4.0 0 0 A″Amano″12 4.0 300 610 A″Amano″12/Alcalase ® 4.0 220 540 Validase AN 4.0 0 20 Validase AN/Alcalase ® 4.0 0 50 ICR-110 4.0 240 490 ICR110/Alcalase ® 4.0 330 580 no enzyme (control) 6.5 80 90 Alcalase ® 6.5 180 330 A″Amano″12 6.5 460 490 A″Amano″12/Alcalase ® 6.5 290 620 Validase AN 6.5 490 730 Validase AN/Alcalase ® 6.5 360 700 ICR-110 6.5 240 440 ICR110/Alcalase ® 6.5 370 420

EXAMPLE 23 Enzymatic Perhydrolysis of a Mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) using a Combination of Lipase and Alcalase® at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-110 (BioCatalytics)), and 20 μL Alcalase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing a mixture of diacetin (250 mM), triacetin (88 mM) and monoacetin (192 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 28). Reactions were also run with lipase alone or Alcalase® alone for comparison of peracetic acid concentrations produced without the combination of lipase and Alcalase®. TABLE 28 Enzymatic Perhydrolysis of a mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) using a Combination of Lipase and Alcalase ® at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 19 44 Alcalase ® 4.0 0 20 A″Amano″12 4.0 150 360 A″Amano″12/Alcalase ® 4.0 130 330 Validase AN 4.0 0 80 Validase AN/Alcalase ® 4.0 0 10 ICR-110 4.0 670 760 ICR110/Alcalase ® 4.0 710 780 no enzyme (control) 6.5 10 10 Alcalase ® 6.5 110 210 A″Amano″12 6.5 190 580 A″Amano″12/Alcalase ® 6.5 170 420 Validase AN 6.5 180 580 Validase AN/Alcalase ® 6.5 190 400 ICR-110 6.5 360 500 ICR110/Alcalase ® 6.5 470 470

EXAMPLE 24 Enzymatic Perhydrolysis of Triacetin Using a Combination of Lipase and Neutrase® at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-110 (BioCatalytics)), and 20 μL Neutrase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing triacetin (250 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minute at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 29). Reactions were also run with lipase alone or Neutrase® alone for comparison of peracetic acid concentrations produced without the combination of lipase and Neutrase®. TABLE 29 Enzymatic Perhydrolysis of Triacetin (250 mM) Using a Combination of Lipase and Neutrase ® at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 10 10 Neutrase ® 4.0 0 0 A”Amano”12 4.0 300 610 A”Amano”12/Neutrase ® 4.0 190 430 Validase AN 4.0 0 20 Validase AN/Neutrase ® 4.0 0 10 ICR-110 4.0 240 490 ICR110/Neutrase ® 4.0 190 430 no enzyme (control) 6.5 125 110 Neutrase ® 6.5 110 300 A”Amano”12 6.5 530 480 A”Amano”12/Neutrase ® 6.5 195 620 Validase AN 6.5 560 720 Validase AN/Neutrase ® 6.5 330 600 ICR-110 6.5 310 430 ICR110/Neutrase ® 6.5 300 390

EXAMPLE 25 Enzymatic Perhydrolysis of a mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) using a Combination of Lipase and Neutrase® at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-110 (BioCatalytics)), and 20 μL Neutrase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing a mixture of diacetin (250 mM), triacetin (88 mM) and monoacetin (192 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minutes at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 30). Reactions were also run with lipase alone or Neutrase® alone for comparison of peracetic acid concentrations produced without the combination of lipase and Neutrase®. TABLE 30 Enzymatic Perhydrolysis of a mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) using a Combination of Lipase and Neutrase ® at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 35 10 Neutrase ® 4.0 50 110 A”Amano”12 4.0 135 310 A”Amano”12/Neutrase ® 4.0 145 320 Validase AN 4.0 0 30 Validase AN/Neutrase ® 4.0 125 400 ICR-110 4.0 655 710 ICR110/Neutrase ® 4.0 515 500 no enzyme (control) 6.5 35 10 Neutrase ® 6.5 50 110 A”Amano”12 6.5 245 460 A”Amano”12/Neutrase ® 6.5 145 390 Validase AN 6.5 235 460 Validase AN/Neutrase ® 6.5 125 320 ICR-110 6.5 415 380 ICR110/Neutrase ® 6.5 515 500

EXAMPLE 26 Enzymatic Perhydrolysis of Triacetin Using a Combination of Lipase and Proteases at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-1 10 (BioCatalytics)), 20 μL Alcalase® (Novozymes), and 20 μL Neutrase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing triacetin (250 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minutes at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 31). Reactions were also run with lipase alone or protease(s) alone for comparison of peracetic acid concentrations produced without the combination of lipase and protease(s). TABLE 31 Enzymatic Perhydrolysis of Triacetin (250 mM) using a Combination of Lipase and Proteases at pH 4.0 and 6.5. peracetic peracetic acid acid (ppm), (ppm), enzyme source pH 5 min 30 min no enzyme (control) 4.0 30 10 Alcalase ® and Neutrase ® 4.0 0 0 A”Amano”12 4.0 360 630 A”Amano”12/Alcalase ®/Neutrase ® 4.0 210 420 Validase AN 4.0 310 540 Validase AN/Alcalase ®/Neutrase ® 4.0 160 380 ICR-110 4.0 300 510 ICR110/Alcalase ®/Neutrase ® 4.0 270 470 no enzyme (control) 6.5 180 310 Alcalase ® and Neutrase ® 6.5 240 480 A”Amano”12 6.5 490 800 A”Amano”12/Alcalase ®/Neutrase ® 6.5 360 720 Validase AN 6.5 470 820 Validase AN/Alcalase ®/Neutrase ® 6.5 460 780 ICR-110 6.5 340 540 ICR110/Alcalase ®/Neutrase ® 6.5 490 560

EXAMPLE 27 Enzymatic Perhydrolysis of a Mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) Using a Combination of Lipase and Proteases at pH 4.0 and 6.5

Reaction mixtures were prepared containing 1 mg lipase (A“Amano”12 (Amano), Validase AN (Valley Research), or ICR-110 (BioCatalytics)), 20 μL Alcalase® (Novozymes), and 20 μL Neutrase® (Novozymes) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing a mixture of diacetin (250 mM), triacetin (88 mM) and monoacetin (192 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minutes at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 32). Reactions were also run with lipase alone or protease(s) alone for comparison of peracetic acid concentrations produced without the combination of lipase and protease(s). TABLE 32 Enzymatic Perhydrolysis of a Mixture of Diacetin (250 mM), Triacetin (88 mM) and Monoacetin (192 mM) Using a Combination of Lipase and Proteases at pH 4.0 and 6.5. peracetic peracetic acid acid (ppm), (ppm), enzyme source pH 5 min 30 min no enzyme (control) 4.0 20 10 Alcalase ® and Neutrase ® 4.0 10 0 A”Amano”12 4.0 190 360 A”Amano”12/Alcalase ®/Neutrase ® 4.0 120 260 Validase AN 4.0 150 270 Validase AN/Alcalase ®/Neutrase ® 4.0 70 230 ICR-110 4.0 490 730 ICR110/Alcalase ®/Neutrase ® 4.0 400 600 no enzyme (control) 6.5 90 170 Alcalase ® and Neutrase ® 6.5 130 260 A”Amano”12 6.5 240 550 A”Amano”12/Alcalase ®/Neutrase ® 6.5 250 560 Validase AN 6.5 280 440 Validase AN/Alcalase ®/Neutrase ® 6.5 270 540 ICR-110 6.5 770 680 ICR110/Alcalase ®/Neutrase ® 6.5 810 670

EXAMPLE 28 Enzymatic Perhydrolysis of Triacetin using a Protease at pH 4.0 and 6.5

Reaction mixtures were prepared containing 5 mg protease (Savinase® 12T, Polarzyme® 12T or Everlase® 12T (Novozymes)) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing triacetin (500 mM) and hydrogen peroxide (1000 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minutes at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 33). TABLE 33 Enzymatic Perhydrolysis of Triacetin (500 mM) using a Protease at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 260 130 Savinase ® 12T 4.0 220 170 Polarzyme ® 12T 4.0 420 40 Everlase ® 12T 4.0 80 380 no enzyme (control) 6.5 170 220 Savinase ® 12T 6.5 480 1240 Polarzyme ® 12T 6.5 550 1940 Everlase ® 12T 6.5 710 1700

EXAMPLE 29 Enzymatic Perhydrolysis of a Mixture of Diacetin (236 mM), Triacetin (83 mM) and Monoacetin (181 mM) using a Protease at pH 4.0 and 6.5

Reaction mixtures were prepared containing 5 mg protease (Savinase® 12T, Polarzymee 12T or Everlasee 12T (Novozymes)) in 1.0 mL of 50 mM buffer (either sodium acetate/acetic acid buffer at pH 4.0, or potassium phosphate buffer at pH 6.5), additionally containing a mixture of diacetin (236 mM), triacetin (83 mM) and monoacetin (181 mM) and hydrogen peroxide (500 mM). After stirring for 5 or 30 minutes at 22° C., a 0.250-mL sample was filtered using a 30,000 NMWL filter (Millipore UltraFree-MC) centrifuged for 2 minutes at 12,000 RPM. A portion of the filtered reaction samples was diluted 1:10 with dd water and analyzed for hydrogen peroxide, and the remaining portion of the sample was directly analyzed for peracid using the HPLC assay method (Table 34). TABLE 34 Enzymatic Perhydrolysis of a Mixture of Diacetin (236 mM), Triacetin (83 mM) and Monoacetin (181 mM) Using a Protease at pH 4.0 and 6.5. peracetic acid peracetic acid enzyme source pH (ppm), 5 min (ppm), 30 min no enzyme (control) 4.0 10 130 Savinase ® 12T 4.0 40 100 Polarzyme ® 12T 4.0 70 80 Everlase ® 12T 4.0 110 60 no enzyme (control) 6.5 350 440 Savinase ® 12T 6.5 185 380 Polarzyme ® 12T 6.5 270 920 Everlase ® 12T 6.5 290 760 

1. A process for producing a concentrated aqueous peracid solution comprising; a) providing a set of peracid reaction components, said components comprising: 1) at least one substrate selected from the group consisting of: i) esters having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₂═C1 to C10 straight chain or branched chain alkyl group, (CH₂CH₂—O)_(n)H or (CH₂CH(CH₃)—O)_(n)H and n=1 to 10; ii) glycerides having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₃ and R₄ are individually H or R₁C(O); and iii) amides having the structure:

wherein R₅ and R₆═H or a C1 to C5 straight chain or branched alkyl group; 2) a source of peroxygen that provides a concentration of at least 500 mM hydrogen peroxide upon combining said reaction components; and 3) at least one enzyme catalyst having perhydrolase activity, wherein said enzyme catalyst is selected from the group consisting of lipases, esterases, proteases, and mixtures thereof; and b) combining said reaction components at a pH of about 2.5 to about 7.5, whereby a concentrated peracid solution is produced within at least about 5 minutes to about 2 hours after combining said reaction components.
 2. The process of claim 1 wherein the pH is 3 to
 7. 3. The process of claim 2 wherein the pH is 4 to 6.5.
 4. The process of claim 1 wherein the concentrated peracid solution has a peracid concentration of at least 10 ppm.
 5. The process of claim 4 wherein the peracid concentration is at least 100 ppm.
 6. The process of claim 5 wherein the peracid concentration is at least 500 ppm.
 7. The process of claim 6 wherein the peracid concentration is at least 1000 ppm.
 8. The process of claim 7 wherein the peracid concentration is at least 5000 ppm.
 9. The process of claim 1 wherein the reaction components comprise at least one lipase and at least one substrate selected from the group consisting of esters, glycerides, and mixtures thereof.
 10. The process of claim 1 or claim 9 wherein said at least one substrate is an ester substrate selected from the group consisting of methyl lactate, ethyl lactate, methyl glycolate, ethyl glycolate, methyl methoxyacetate, ethyl methoxyacetate, methyl 3-hydroxybutyrate, ethyl 3-hydroxybutyrate, and mixtures thereof.
 11. The process of claim 1 or claim 9 wherein the said at least one substrate is a glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, and mixtures thereof.
 12. The process of claim 11 wherein said glyceride substrate is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.
 13. The process of claim 1 wherein said at least one enzyme catalyst is at least one lipase produced by an organism selected from the genera Aspergillus, Rhizopus, Penicillium, Candida, Pseudomonas, Mucor, Thermomyces, Alcaligenes, and Sus.
 14. The process of claim 13 wherein said at least one lipase is produced by an organism selected from the group consisting of Aspergillus sp., Aspergillus niger, Rhizopus sp., Rhizopus oryzae, Penicillium sp. I, Penicillium sp. II, Candida rugosa, Candida antartica, Pseudomonas cepacia, Pseudomonas fluorescens, Thermomyces lanuginosus, Mucor miehei, and Alcaligenes sp.
 15. The process of claim 14 wherein said lipase is selected from the group consisting of Aspergillus sp. lipase, Aspergillus niger lipase, Rhizopus oryzae lipase, Candida rugosa lipase, Candida antartica lipase A, Candida antartica lipase B, Pseudomonas sp. lipase, Pseudomonas cepacia lipase, Pseudomonas fluorescens lipase, Thermomyces lanuginosus lipase, Mucor miehei lipase, Alcaligenes sp. lipase, and mixtures thereof.
 16. The process of claim 15 wherein said lipase is selected from the group consisting of BioCatalytics ICR-101 Aspergillus sp. lipase, BioCatalytics ICR-102 Rhizopus sp. lipase, BioCatalytics ICR-103 Rhizopus oryzae lipase, BioCatalytics ICR-104 Penicillium sp. I lipase, BioCatalytics ICR-105 Penicillium sp. II lipase, BioCatalytics ICR-106 Candida rugosa lipase, BioCatalytics ICR-107 Pseudomonas cepacia lipase, BioCatalytics ICR-108 Pseudomonas sp. lipase, BioCatalytics ICR-109 Pseudomonas fluorescens lipase, BioCatalytics ICR-110 Candida antartica lipase B, BioCatalytics ICR-111 Candida sp. lipase, BioCatalytics ICR-112 Candida antartica lipase A, BioCatalytics ICR-113 Pseudomonas sp. lipase, BioCatalytics ICR-114 porcine pancreas lipase, BioCatalytics ICR-115 Thermomyces languinosus lipase, BioCatalytics ICR-116 Mucor miehei lipase, BioCatalytics ICR-117 Alcaligenes sp. lipase, BioCatalytics IMB-111 immobilized Candida antartica lipase B, Amano Lipase AY 30 Candida rugosa lipase, Amano Lipase R Penicillium roqueforti lipase, Amano Lipase F-AP15 Rhizopus oryzae lipase, Amano Lipase M 10 Mucor javanicus lipase, Amano Lipase A 12 Aspergillus niger lipase, Amano Lipase G 50 Penicillium camembertii lipase, Amano F-DS Rhizopus oryzae lipase, Amano DS Aspergillus niger lipase, Novozym CALB L Candida antartica lipase B, Novozym 435 immobilized Candida antartica lipase B, and Novozym Palatase 20000L Aspergillus oryzae lipase, Lipozyme TL Thermomyces lanuginosus lipase, Chirazyme L2 Candida antartica lipase B, Validase AN Aspergillus niger lipase, Dietrenz CR Candida rugosa lipase, Enzeco MLC Aspergillus niger lipase, and mixtures thereof.
 17. The process of claim 15 wherein said lipase is selected from the group consisting of Candida antartica lipase B and Aspergillus niger lipase.
 18. The process of claim 1 wherein said at least one enzyme catalyst is at least one protease.
 19. The process of claim 18 wherein said at least one substrate is selected from the group of esters, glycerides, and mixtures thereof.
 20. The process of claim 19 wherein said substrate is an ester substrate selected from the group consisting of methyl lactate, ethyl lactate, methyl glycolate, ethyl glycolate, methyl methoxyacetate, ethyl methoxyacetate, methyl 3-hydroxybutyrate, ethyl 3-hydroxybutyrate, and mixtures thereof.
 21. The process of claim 19 wherein said substrate is a glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, and mixtures thereof.
 22. The process of claim 21 wherein the glyceride substrate is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.
 23. The process of claim 18 wherein said at least one substrate is an amide selected from the group consisting of acetamide, diacetamide, and mixtures of acetamide and diacetamide.
 24. The process of claim 18 wherein said at least one protease is produced by an organism selected from the genera Aspergillus, Rhizopus, Bacillus, Carica, Ananas, Streptomyces, Tritirachium, and Sus.
 25. The process of claim 24 wherein said protease is produced from an organism selected from the group consisting of Aspergillus saitoi, Rhizopus sp., Bacillus sp., Bacillus subtilis, Bacillus amyloliquefaciens, Bacillus licheniformis, Bacillus lentus, Sus scrofa, Carica papaya, Ananas comosus, Streptomyces griseus, and Tritirachium album.
 26. The process of claim 25 wherein said protease is selected from the group consisting of Aspergillus saitoi protease type XIII, Rhizopus sp. protease type XVIII, Bacillus sp. protease, Sus scrofa pepsin, Carica papaya Chymopapain, Carica papaya papain, Ananas comosus bromelain, Streptomyces griseus Pronase, Tritirachium album Proteinase K, Alcalase®, Neutrase®, Everlase®, Polarzyme®, Savinase®, and mixtures thereof.
 27. The process of claim 26 wherein said protease is selected from the group consisting of Streptomyces griseus Pronase, Tritirachium album Proteinase K, Alcalase®, Neutrase®, and mixtures thereof.
 28. The process of claim 18 wherein said at least one protease has prion-degrading activity and perhydrolase activity
 29. The process of claim 1 wherein the reaction components comprise at least one lipase and at least one prion-degrading protease.
 30. The process of claim 29 wherein the prion-degrading protease is selected from the group consisting of Proteinase K, Pronase, Alcalase®, Neutrase®, and mixtures thereof.
 31. The process of claim 1 wherein the peracid produced is selected from the group consisting of peracetic acid, perbutyric acid, perlactic acid, perglycolic acid, permethoxyacetic acid, per-p-hydroxybutyric acid, peroctanoic acid, and mixtures thereof.
 32. The process of claim 31 wherein the peracid is peracetic acid.
 33. A method for disinfecting a locus having a concentration of microorganisms or viruses or combinations thereof, said method comprising: a) providing a set of peracid reaction components, said components comprising: 1) at least one substrate selected from the group consisting of: i) esters having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₂═C1 to C10 straight chain or branched chain alkyl group, (CH₂CH₂—O)_(n)H or (CH₂CH(CH₃)—O)_(n)H and n=1 to 10; ii) glycerides having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₃ and R₄ are individually H or R₁C(O); and iii) amides having the structure:

wherein R₅ and R₆═H or a C1 to C5 straight chain or branched alkyl group; 2) a source of peroxygen that provides a concentration of at least 500 mM hydrogen peroxide upon combining said reaction components; and 3) at least one enzyme catalyst having perhydrolase activity, wherein said enzyme catalyst is selected from the group consisting of lipases, esterases, proteases, and mixtures thereof; b) combining said reaction components at a pH of 2.5 to 7.5, whereby a concentrated aqueous peracid solution is formed having a peracid concentration of at least 10 ppm within at least about 5 minutes to about 2 hours of combining said reaction components; c) optionally diluting the said aqueous peracid solution; and d) contacting said locus with the aqueous peracid solution produced in step b) or step c) whereby the concentration of said microorganisms is reduced at least 3-log.
 34. The method of claim 33 wherein the locus is contacted with the aqueous peracid solution produced in step b) or step c) within about 48 hours of combining said reaction components.
 35. The method of claim 34 wherein the locus is contacted with the aqueous peracid solution produced in step b) or step c) within about 24 hours of combining said reaction components.
 36. The method according to claim 33 wherein the concentration of said microorganisms is reduced at least 6-log.
 37. The method of claim 33 wherein the pH is 3 to
 7. 38. The method of claim 37 wherein the pH is 4 to 6.5.
 39. The method of claim 33 wherein the peracid concentration is at least 100 ppm.
 40. The method of claim 39 wherein the peracid concentration is at least 500 ppm.
 41. The method of claim 40 wherein the peracid concentration is at least 1000 ppm.
 42. The method of claim 41 wherein the peracid concentration is at least 5000 ppm.
 43. The method of claim 33 wherein the reaction components comprise at least one lipase and at least one substrate selected from the group consisting of esters, glycerides, and mixtures thereof.
 44. The method of claims 33 or 43 wherein said at least one substrate is an ester substrate selected from the group consisting of methyl lactate, ethyl lactate, methyl glycolate, ethyl glycolate, methyl methoxyacetate, ethyl methoxyacetate, methyl 3-hydroxybutyrate, ethyl 3-hydroxybutyrate, and mixtures thereof.
 45. The method of claims 33 or 43 wherein said at least one substrate is a glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, and mixtures thereof.
 46. The method of claim 45 wherein said glyceride substrate is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.
 47. The method of claim 33 wherein said at least one enzyme catalyst is at least one lipase produced by an organism selected from the genera Aspergillus, Rhizopus, Penicillium, Candida, Pseudomonas, Mucor, Thermomyces, Alcaligenes, and Sus.
 48. The method of claim 47 wherein said at least one lipase is produced by an organism selected from the group consisting of Aspergillus sp., Aspergillus niger, Rhizopus sp., Rhizopus oryzae, Penicillium sp. I, Penicillium sp. II, Candida rugosa, Candida antartica, Pseudomonas cepacia, Pseudomonas fluorescens, Thermomyces lanuginosus, Mucor miehei, and Alcaligenes sp.
 49. The method of claim 48 wherein said at least one lipase is selected from the group consisting of Aspergillus sp. lipase, Aspergillus niger lipase, Rhizopus oryzae lipase, Candida rugosa lipase, Candida antartic lipase A, Candida antartica lipase B, Pseudomonas sp. lipase, Pseudomonas cepacia lipase, Pseudomonas fluorescens lipase, Thermomyces lanuginosus lipase, Mucor miehei lipase, Alcaligenes sp. lipase, and mixtures thereof.
 50. The method of claim 49 wherein said at least one lipase is selected from the group consisting of BioCatalytics ICR-101 Aspergillus sp. lipase, BioCatalytics ICR-102 Rhizopus sp. lipase, BioCatalytics ICR-103 Rhizopus oryzae lipase, BioCatalytics ICR-104 Penicillium sp. I lipase, BioCatalytics ICR-105 Penicillium sp. II lipase, BioCatalytics ICR-106 Candida rugosa lipase, BioCatalytics ICR-107 Pseudomonas cepacia lipase, BioCatalytics ICR-108 Pseudomonas sp. lipase, BioCatalytics ICR-109 Pseudomonas fluorescens lipase, BioCatalytics ICR-110 Candida antartica lipase B, BioCatalytics ICR-111 Candida sp. lipase, BioCatalytics ICR-112 Candida antartica lipase A, BioCatalytics ICR-113 Pseudomonas sp. lipase, BioCatalytics ICR-114 porcine pancreas lipase, BioCatalytics ICR-115 Thermomyces languinosus lipase, BioCatalytics ICR-116 Mucor miehei lipase, BioCatalytics ICR-117 Alcaligenes sp. lipase, BioCatalytics IMB-111 immobilized Candida antartica lipase B, Amano Lipase AY 30 Candida rugosa lipase, Amano Lipase R Penicillium roqueforti lipase, Amano Lipase F-AP15 Rhizopus oryzae lipase, Amano Lipase M 10 Mucor javanicus lipase, Amano Lipase A 12 Aspergillus niger lipase, Amano Lipase G 50 Penicillium camembertii lipase, Amano F-DS Rhizopus oryzae lipase, Amano DS Aspergillus niger lipase, Novozym CALB L Candida antartica lipase B, Novozym 435 immobilized Candida antartica lipase B, and Novozym Palatase 20000L Aspergillus oryzae lipase, Lipozyme TL Thermomyces lanuginosus lipase, Chirazyme L2 Candida antartica lipase B, Validase AN Aspergillus niger lipase, Dietrenz CR Candida rugosa lipase, Enzeco MLC Aspergillus niger lipase, and mixtures thereof.
 51. The method of claim 49 wherein said at least one lipase is selected from the group consisting of Candida antartica lipase B and Aspergillus niger lipase.
 52. The method of claim 33 wherein the enzyme catalyst is at least one protease.
 53. The method of claim 52 wherein the substrate is at least one amide substrate selected from the group consisting of acetamide, diacetamide, and mixtures of acetamide and diacetamide.
 54. The method of claim 52 wherein the substrate is at least one glyceride substrate selected from the group consisting of monoacetin, diacetin, triacetin, diacetin, monobutyrin, dibutyrin, tributyrin, glyceryl monooctanoate, glyceryl dioctanoate, glyceryl trioctanoate, and mixtures thereof.
 55. The method of claim 54 wherein said is at least one glyceride substrate is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.
 56. The method of claim 52 wherein said at least one protease is produced from an organism selected from the genera Aspergillus, Rhizopus, Bacillus, Carica, Ananas, Streptomyces, Tritirachium, and Sus.
 57. The method of claim 56 wherein said at least one protease is produced from the organism selected from the group consisting of Aspergillus saitoi, Rhizopus sp., Bacillus sp., Bacillus subtilis, Bacillus licheniformis, Bacillus amyloliquefaciens, Bacillus lentus, Sus scrofa, Carica papaya, Ananas comosus, Streptomyces griseus, and Tritirachium album.
 58. The method of claim 57 wherein said at least one protease is selected from the group consisting of Aspergillus saitoi protease type XII, Rhizopus sp. protease type XVIII, Bacillus sp. protease, Sus scrofa pepsin, Carica papaya Chymopapain, Carica papaya papain, Ananas comosus bromelain, Streptomyces griseus Pronase, Tritirachium album proteinase K, Alcalase®, Neutrase®, Everlase®, Polarzyme®, Savinase®, and mixtures thereof.
 59. The method of claim 58 wherein said at least one protease is selected from the group consisting of Streptomyces griseus Pronase, Tritirachium album Proteinase K, Alcalase®, Neutrase®, and mixtures thereof.
 60. The method of claim 52 wherein said at least one protease has prion-degrading activity and perhydrolase activity.
 61. The method of claim 33 wherein the reaction components comprise at least one lipase and at least on prion-degrading protease.
 62. The method of claim 61 wherein the reaction components comprise at least one lipase and at least one prion-degrading protease selected from the group consisting of Proteinase K, Pronase, Alcalase®, Neutrase®, and mixtures thereof.
 63. The method of claim 33 wherein the peracid produced is selected from the group consisting of peracetic acid, perbutyric acid, perlactic acid, perglycolic acid, permethoxyacetic acid, per-β-hydroxybutyric acid, peroctanoic acid, and mixtures thereof.
 64. The method of claim 63 wherein the peracid is peracetic acid.
 65. A method for decontaminating or disinfecting a locus contaminated with one or more pathogens including an infective prion or prion particle comprising a) providing a set of peracid reaction components, said components comprising: 1) at least one substrate selected from the group consisting of: i) esters having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₂═C1 to C10 straight chain or branched chain alkyl group, (CH₂CH₂—O)_(n)H or (CH₂CH(CH₃)—O)_(n)H and n=1 to 10; ii) glycerides having the structure

wherein R₁═C1 to C10 straight chain or branched chain alkyl optionally substituted with an hydroxyl or a C1 to C4 alkoxy group and R₃ and R₄ are individually H or R₁C(O); and iii) amides having the structure:

wherein R₅ and R₆═H or a C1 to C5 straight chain or branched alkyl group; 2) a source of peroxygen that provides a concentration of at least 500 mM hydrogen peroxide upon combining said reaction components; and 3) at least one enzyme catalyst having perhydrolase activity, wherein said enzyme catalyst is selected from the group consisting of lipases, proteases, and mixtures thereof; 4) at least one prion-degrading protease wherein one or more of the prion-degrading proteases may be the same as the enzyme catalyst providing the perhydrolase activity in (a)(3); b) combining said reaction components at a pH of 2.5 to 7.5, whereby a concentrated peracid solution is produced having a peracid concentration of at least 10 ppm within at least about 5 minutes to about 2 hours of combining said reaction components; and c) optionally diluting said peracid solution produced in step (b). d) contacting a locus contaminated with a microorganism, a virus, a prion or prion particle, or a combination thereof with the aqueous peracid solution produced in step b) or step c) whereby said locus is disinfected and said prion particle is degraded.
 66. The method of claim 65 wherein the locus is contacted with the aqueous peracid solution produced in step b) or step c) within about 48 hours of combining said reaction components.
 67. The method of claim 66 wherein the locus is contacted with the aqueous peracid solution produced in step b) or step c) within about 24 hours of combining said reaction components.
 68. The method of claim 65 wherein said at least one protease comprises a mixture of at least two proteases.
 69. The method of claim 68 wherein said mixture of at least two proteases comprises Pronase® and Proteinase K.
 70. The method of claim 68 wherein said mixture of at least two proteases comprises Alcalase® and Neutrase®.
 71. The method of claim 65 wherein the pH is 3 to
 7. 72. The method of claim 66 wherein the pH is 4 to 6.5.
 73. The method of claim 65 wherein the peracid concentration is at least 100 ppm.
 74. The method of claim 73 wherein the peracid concentration is at least 500 ppm.
 75. The method of claim 74 wherein the peracid concentration is at least 1000 ppm.
 76. The method of claim 75 wherein the peracid concentration is at least 5000 ppm.
 77. The method of claim 65 wherein the reaction components further comprises at least one surfactant.
 78. The method of claim 77 wherein said at least one surfactant is sodium dodecylsulfate.
 79. The method of claim 65 further comprising the step of contacting said locus with at least one surfactant.
 80. The method of claims 65, 77, or 79 wherein the method further comprises the step of heating said locus to a temperature of at least 80° C. for a period of time from at least 1 minute to 48 hours before or after contacting said locus with said aqueous peracid solution.
 81. A concentrated peracid solution produced in situ by the process of claim 1, wherein said solution includes at least one protease suitable for prion degradation.
 82. A multifunctional disinfectant composition comprising the concentrated peracid solution produced by the process of claim 1, wherein said composition is suitable for prion degradation, use as a biocide, use as a virucide, or combinations thereof.
 83. A biocidal composition comprising components suitable for producing peracid in situ, wherein said components comprise one or more prion-degrading enzymes, a suitable substrate, at least one enzyme having perhydrolase activity, and a source of peroxygen.
 84. The composition of claim 83, wherein said at least one enzyme having perhydrolase activity is said one or more prion-degrading enzymes.
 85. The composition of claim 84, wherein said one or more prion-degrading enzymes is at least one protease isolated from a host organism selected from the group of Aspergillus saitoi, Rhizopus sp., Bacillus sp., Bacillus subtilis, Bacillus licheniformis, Bacillus amyloliquefaciens, Bacillus lentus, Sus scrofa, Carica papaya, Ananas comosus, Streptomyces griseus, and Tritirachium album.
 86. The composition of claim 85 wherein the protease is selected from the group consisting of Pronase®, Proteinase K, Alcalase® and Neutrase®.
 87. The composition of claim 86 wherein the protease is selected from the group consisting of Alcalase® and Neutrase®.
 88. The composition of claim 86 wherein said one or more prion-degrading proteases is a mixture of at least two proteases.
 89. The composition of claim 88 wherein said mixture of proteases comprises Pronase® and Proteinase K.
 90. The composition of claim 89 wherein said mixture of proteases comprises Alcalase® and Neutrase®.
 91. The composition of any one of claims 87, 88, 89, and 90 wherein the peracid produced in situ is peracetic acid.
 92. The composition of claim 91 wherein the suitable substrate used to produce peracetic acid in situ is selected from the group consisting of monoacetin, diacetin, triacetin, and mixtures thereof.
 93. The composition of claim 92 wherein the peracetic acid produced in situ is at least 10 ppm. 